US3870051A - Urinary control - Google Patents

Urinary control Download PDF

Info

Publication number
US3870051A
US3870051A US354910A US35491073A US3870051A US 3870051 A US3870051 A US 3870051A US 354910 A US354910 A US 354910A US 35491073 A US35491073 A US 35491073A US 3870051 A US3870051 A US 3870051A
Authority
US
United States
Prior art keywords
muscle
bladder
intensity
signals
muscles
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US354910A
Inventor
Giles Skey Brindley
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
National Research Development Corp UK
Original Assignee
National Research Development Corp UK
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by National Research Development Corp UK filed Critical National Research Development Corp UK
Application granted granted Critical
Publication of US3870051A publication Critical patent/US3870051A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61NELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N1/00Electrotherapy; Circuits therefor
    • A61N1/18Applying electric currents by contact electrodes
    • A61N1/32Applying electric currents by contact electrodes alternating or intermittent currents
    • A61N1/36Applying electric currents by contact electrodes alternating or intermittent currents for stimulation
    • A61N1/36007Applying electric currents by contact electrodes alternating or intermittent currents for stimulation of urogenital or gastrointestinal organs, e.g. for incontinence control
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S128/00Surgery
    • Y10S128/25Artificial sphincters and devices for controlling urinary incontinence

Definitions

  • the invention more particularly, but not exclusively, concerns urinary control for persons having disorders of neurological origin whereby they are unable to empty urine from the bladder by normal action of the bladder muscle, or unable to retain urine in the bladder by normal action of the sphincter, or, as is often the case, are unable to do either.
  • the present invention affords similar urinary control by stimulation of the relevant muscles through electrodes implanted in the associated parts of the sacral ventral roots, normally numbers three and four, left and right.
  • the muscles in question will be referred to hereinafter for convenience simply as the bladder muscle and the sphincter muscle.
  • the former is intended to denote the detrusor muscle of the bladder, and the latter all of those striated muscles that contribute to closing the urethra.
  • the principal one of these last muscles is the external sphincter of the urethra, but other pelvic muscles are also considered to be involved.
  • An advantage of the presently proposed control is that the sacral ventral roots are free from sensory fibres with the result that stimulation is unlikely to lead to painJAlso, it is more economic in terms of power requirements to stimulate the sacral ventral roots than the muscles directly or the motor nerve fibres in them.
  • the sacral ventral'roots in question comprise tightly packed bundles including those which govern the activity of the bladder muscle and those which govern the activity of the sphincter muscle. Accordingly, unless it proves possible to separate the respective fibres, and this seems an impossible task on the basis of existing knowledge, it is necessary to adopt a mode of differential stimulation.
  • the invention involves one mode of differential stimulation which stems from the fact that the bladder muscle relaxes slowly after stimulation to contraction, while the sphincter muscle relaxes very rapidly in comparison.
  • each active signal will normally comprise a pulse train and the relevant interruption period is the inter-train interval.
  • Another mode of differential stimulation stems from the fact that the sacral ventral root fibres governing the activity of the bladder muscle are small compared to those for the sphincter muscle, and it follows that the latter fibres are more sensitive to electrical stimulation than theformer. Thus, it ispossible to stimulate the fibres at an intensity which causes contraction of the sphincter muscle but not the bladder muscle. Again, this stimulation will normally involve the use of a pulse train signal.
  • the power requirements for the two modes of stimulation are sufficiently low, namely, low intensity for long durations and high intensity for short durations, that implantation of suitable micro-circuits with battery power supplies is possible.
  • This can be effected by use of a radio transmitter/receiver arrangement as more generally de scribed in US. Pat. No. 3,699,970 whereby an externally located transmitter is operated to energise an implanted receiver.
  • the use of such arrangements would allow both the hold and empty modes of control to be individually powered from without the body and so obviate the need for any implantation of power supplies.
  • the present development has involved implementation with a compromise between these effective extremes of maximum and minimum implantation.
  • the hold mode of control is provided by way of total implantation, and the empty mode by way of a transmitter/receiver arrangement which also serves to inhibit the hold mode.
  • This overall arrangement is presently considered to represent an optimum in convenience to the beneficiary.
  • the illustrated embodiment is in two parts denoted at 10 and 11 of which the first is implantable and the second employed externally of the body. Also these two parts 10 and 11 are themselves functionally subdivided into portions 10A, 10B and 11A, 118, although thissubdivision does not necessarily involve physical separation.
  • the implantable portion A is the circuit which provides the hold mode of control referred to above and comprises a complementary multivibrator stage operable to generate a pulse train of twenty pulses per second which are applied through a buffer stage 21 and output stage 22 to stimulating electrodes 23A.
  • the electrodes 23A are located adjacent the relevant ventralsacral roots by use of electrode terminal devices such as describedin US. Pat. No.
  • resistor RlA 3718,134 and the tissue load at the electrodes is denoted by broken line resistor RlA;
  • This circuit is powered by a mercury cell 24, resistor R2 in the multivibrator stage is chosen so that fifty microsecond pulses are generated, and the potentiometer R3 affords adjustment of the output pulse intensity to a low level at which only the sphincter mus cle is contracted.
  • Potentiometer R3 is preferably ad- 'justable post-operatively from without the body and this can be effected by use of a magnetic coupling.
  • the remaining components of the relevant circuit constitute an inhibiting stage 25 in the form of a simple radio receiver which is actuated in response to the external portion 11A to hold the multivibrator transistor switched off.
  • the implantable portion 108 is also of simple radio receiver form and serves, in response to the external portion 11B, to energise further stimulating electrodes 238, in response to the external portion 11B.
  • the external portions 11A, 11B are radio transmitters and it is unnecessary to consider more detailed circuit design since these portions can be of any suitable form to serve the relevant function requirements.
  • the portion 118 which as mentioned earlier is to provide a relatively high intensity, interrupted pulse train signal.
  • the portion 118 comprised two multivibrators connected in cascade, with the first activating the second for a period of 120 milliseconds each 1 /2 seconds, the second generating 12 /2 millisecond pulses at 9 /2 milliseconds separation during each period of activation, and the last-mentioned pulses gating the radio frequency output of the relevant transmitter.
  • portion 11A which is operated at the same time as portion 118 to provide a radio signal .to inhibit the portion 10A.
  • a method of urinary control which comprises applying an electricalsignal of continuous pulse train form to'the sacralventral roots,.said sacral ventral roots communicating with the sphincter muscle and bladder muscle, thereby causing the step of contracting said sphincter muscle while said bladder muscle is relaxed.
  • each of said pulse trains comprises pulses of about /2 millisecond duration each 10 milliseconds.
  • a method of urinary control which comprises alternatively applying two different pulsatile electrical signals to the sacral ventral roots, said sacral ventral roots communicating with the sphincter muscle and bladder muscle to thereby cause the step of stimulating said muscles, one of said signals being of lower intensity and higher repetition rate for causing the step of contracting said sphincter muscle while said bladder muscle is relaxed, and the other signal being of higher intensity and lower repetition rate for causing the step of contraction of both of said muscles during each pulse and to cause the further step of maintaining said bladder muscle contracted during part of successive interpulse periods when said sphincter muscle is relaxed.
  • a method of urinary control in primates comprising:
  • the signals are of a first intensity for the step of contracting the urethra closing muscles, but not contracting the bladder detrusor muscle, and including the step of spacing the first intensity pulses such that the urethra closing muscles do not become substantially relaxed between pulses;
  • the signals are of a second intensity higher than said first intensity signals for causing the step of contracting both the urethra closing muscles and the bladder detrusor muscle
  • electrode means disposed for stimulating the third and fourth, left and right sacral ventral motor nerve fibre roots, without substantially stimulating sensory nerve fibres;
  • multivibrator means and an electrical power supply therefor for emitting said first intensity signals and a connection for communicating these signals to said electrode means;
  • receiver means for receiving a command signal from outside the subject primate and connected to the inhibiting means for commanding same;
  • multivibrator means for emitting said second intensity signals and a connection for communicating these signals to said electrode means
  • receiver means for receiving a command signal from outside the subject primate and connected to the multivibrator means to emit said second intensity signals
  • changing modes from the first to the second comprises: sending command signals from outside the subject primate to the receiver means of (d) and to the receiver means of (f); and
  • the implanted multivibrator means of (b) includes electrical output intensity adjustment means and the method further comprises: post operatively adjusting the intensity of signals provided by the implanted multivibrator means of (b) by adjusting the intensity adjustment means to ensure desired first mode operation wherein there occurs contraction of the striated, sphincter muscles which contribute to closing the urethra without substantially contracting the bladder detrusor muscle.
  • Urinary control apparatus comprising:
  • a. stimulating electrode devices adapted for connection to the sacral ventral roots
  • a first electrical circuit means operable to generate a low intensity, continuous pulse train signal, which circuit means is connected to said electrode devices to energize the same;
  • a second electrical circuit means operable to generate a high intensity, interrupted pulse train signal, which circuit means is connected to said electrode devices to energize the same;
  • said electrode devices and at least part of both said first and second circuit means being adapted for bodily implantation, and at least part of said activating means being for use outside the body.
  • Urinary control apparatus comprising:
  • a, stimulating electrode devices adapted for connection to the sacral ventral roots
  • an implantable electric circuit means including a power source, operable to generate a low intensity continuous pulse train signal, which circuit means is connected to said electrode devices to energize the same;
  • radio transmitter means for use outside the body operable to generate a first signal including at least a high intensity interrupted pulse train and a second signal;
  • an implantable second radio receiver means operable in response to said second signal and connected to said electric circuit to inhibit operation of the same.
  • Apparatus for effecting urinary control in primates by applying pulsing electrical signals to the sacral ventral roots which control contraction of the detrusor muscle for the bladder and the striated, sphincter muscles which contribute to closing the urethra, in two different modes;
  • the signals are of a low intensity so as to contract the urethra closing muscles, but not to contract the bladder detrusor muscle, and wherein these low intensity signals are of such spacing between pulses that the urethra closing muscles do not become substantially relaxed between pulses;
  • the signals are of a different intensity higher than said low intensity signals so as to contract both the urethra closing muscles and the bladder detrusor muscle, but of such spacing between pulses, that the urethra closing muscles, but not the bladder detrusor muscle become sufficiently relaxed between pulses, that pressure exerted on the bladder by the detrusor muscle in between pulses when the urethra closing muscles have relaxed, forces urine from the bladder and out through the urethra;
  • said apparatus comprising a surgical implant which includes:
  • a. electrode means being disposed, when implanted,
  • multivibrator means including an electrical power supply therefor, for emitting said low intensity signals and a connection for communicating these signals to said electrode means;
  • receiver means for receiving the first command signal from outside the subject primate and connected to the inhibiting means for controlling same;
  • multivibrator means for emitting said higher intensity signals and a connection for communicating these signals to said electrode means
  • receiver means for receiving a second command signal from outside the subject primate and connected to the multivibrator means of (e) for commanding and powering that multivibrator means to emit said higher intensity signals;
  • apparatus further comprising external transmitter means for sending said first and second command signals

Landscapes

  • Health & Medical Sciences (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Radiology & Medical Imaging (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • External Artificial Organs (AREA)
  • Electrotherapy Devices (AREA)
  • Prostheses (AREA)

Abstract

Urinary control by electrical stimulation of the sphincter and bladder muscles is effected by way of the sacral ventral roots, selection in the resultant muscle action being effected by use of discriminating signal forms. Sphincter closure action is effected by use of a low intensity pulse train whereby the sphincter is stimulated but not the bladder and so incontinence is avoided. Bladder muscle action to cause micturation is effected by use of a higher intensity pulse train whereby both muscles are stimulated during each pulse train, but during each interruption the sphincter relaxes while the bladder remains contracted.

Description

United States Patent 1191 Brindley Mar. 11, 1975 1 URINARY CONTROL 3,650,276 3/1972 Brughele et a1. 128/419 1-: 3,667,477 6 1972 S t l. 128 419 E [75] Inventor: Giles Skey Brindley, London, usse et a I England Przmary Exammer--W1ll1am E. Kamm [73] Assignee: National Research Development Attorney, Agent, or FirmCushman, Darby &
Corporation, London, England Cushman 22 Pl d: A 26, 1973 1 pr 57 ABSTRACT [2]] Appl' 354910 Urinary control by electrical stimulation of the sphincter and bladder muscles is effected by way of the sa- [30] Foreign Application Priority Data cral ventral roots, selection in the resultant muscle ac- Apr. 27, 1972 Great Britain 19583/72 tion being effected y use of discriminating Signal forms. Sphincter closure action is effected b use of a y 5 Clmmu 128/422, 128/419 5, 128/1316 25 low mtensity pulse train whereby the sphincter is stim- 511 1111. C1 A61n 1/36 but not the bladder and so incontinence is [58] Field of Search U 128/419 E, 419 R, 42] avoided; Bladder muscle action to cause micturation is 128/422v DIG. 25 effected by use of a higher intensity pulse train whereby both muscles are stimulated during each [56] References Cited pulse train, but during each interruption the sphincter UNITED STATES PATENTS relaxes while the bladder remains contracted. 3.236.240 2/l966 Bradley 128/419 E 12 Claims, 1 Drawing Figure 1 l 7 i I H M L 53 H5 2 2 i C a w J A: B6 E R9 772 B7 247 I? 4 'vv/ 23A l X as? B5 1 1 71/1 R/B'Z J C1 r 5 i l 1 l i 3 l TRANSMITTER/ 775 7/) INITIATING HIGH INTENSITY SHORT BURST PULSING\ INHIBITING LOW INTENSITY STEADY PULSING i l g/TRANSMTTER URINARY CONTROL BACKGROUND OF THE INVENTION This invention concerns urinary control and more particularly such control involving electrical stimula tion by way of implanted electrodes. Also, the invention more particularly, but not exclusively, concerns urinary control for persons having disorders of neurological origin whereby they are unable to empty urine from the bladder by normal action of the bladder muscle, or unable to retain urine in the bladder by normal action of the sphincter, or, as is often the case, are unable to do either.
Various attempts have been made in the past to effect urinary control in the presence of such disorders by direct stimulation of appropriate muscles through electrodes implanted on the muscle to stimulate the as sociated motor nerve fibres. However, relatively large currents are required to effect the desired muscle contractions and, because the relevant motor nerve fibres are normally in close proximity with sensory fibres, stimulation is frequently associated with pain.
SUMMARY OF THE INVENTION In a more general aspect, the present invention, on the other hand, affords similar urinary control by stimulation of the relevant muscles through electrodes implanted in the associated parts of the sacral ventral roots, normally numbers three and four, left and right. The muscles in question will be referred to hereinafter for convenience simply as the bladder muscle and the sphincter muscle. The former is intended to denote the detrusor muscle of the bladder, and the latter all of those striated muscles that contribute to closing the urethra. The principal one of these last muscles is the external sphincter of the urethra, but other pelvic muscles are also considered to be involved.
An advantage of the presently proposed control is that the sacral ventral roots are free from sensory fibres with the result that stimulation is unlikely to lead to painJAlso, it is more economic in terms of power requirements to stimulate the sacral ventral roots than the muscles directly or the motor nerve fibres in them.
However, the sacral ventral'roots in question comprise tightly packed bundles including those which govern the activity of the bladder muscle and those which govern the activity of the sphincter muscle. Accordingly, unless it proves possible to separate the respective fibres, and this seems an impossible task on the basis of existing knowledge, it is necessary to adopt a mode of differential stimulation.
The invention involves one mode of differential stimulation which stems from the fact that the bladder muscle relaxes slowly after stimulation to contraction, while the sphincter muscle relaxes very rapidly in comparison. Thus, it is possible to stimulate the relevant fibres with electrical signals of interrupted form so that both muscles are contracted during each active signal period, while the bladder muscle remains contracted and the sphincter muscle is relaxed to afford micturition during at least a part of the signal interruption period. In practice each active signal will normally comprise a pulse train and the relevant interruption period is the inter-train interval.
Another mode of differential stimulation stems from the fact that the sacral ventral root fibres governing the activity of the bladder muscle are small compared to those for the sphincter muscle, and it follows that the latter fibres are more sensitive to electrical stimulation than theformer. Thus, it ispossible to stimulate the fibres at an intensity which causes contraction of the sphincter muscle but not the bladder muscle. Again, this stimulation will normally involve the use of a pulse train signal.
It will be normal for the purposes of the earliermentioned more particular application of the invention to employ both of these modes of differential control with the second mode being employed to hold the sphincter normally contracted except when the first mode is employed to empty the bladder.
As clarification, useful mention can be made of practical development of the invention to date. This development has led to urinary control apparatus for which the normal or hold mode involves stimulation by application of a relatively low intensity pulse train signal having a pulse repetition rate of about twenty per second, and the micturition or empty mode involves stimulation by application of a relatively high intensity, interrupted pulse train signal in which each train comprises about twelve pulses in a relatively short burst each 1 /2 seconds.
Regarding practical implementation of the invention: the power requirements for the two modes of stimulation are sufficiently low, namely, low intensity for long durations and high intensity for short durations, that implantation of suitable micro-circuits with battery power supplies is possible. However, it is necessary to provide some facility, controllable from without the body, to afford switching between the hold andempty modes of control. This can be effected by use of a radio transmitter/receiver arrangement as more generally de scribed in US. Pat. No. 3,699,970 whereby an externally located transmitter is operated to energise an implanted receiver. Indeed, the use of such arrangements would allow both the hold and empty modes of control to be individually powered from without the body and so obviate the need for any implantation of power supplies.
In practice the present development has involved implementation with a compromise between these effective extremes of maximum and minimum implantation. In this compromise, the hold mode of control is provided by way of total implantation, and the empty mode by way of a transmitter/receiver arrangement which also serves to inhibit the hold mode. This overall arrangement is presently considered to represent an optimum in convenience to the beneficiary.
BRIEF DESCRIPTION OF THE DRAWING For completeness in providing a clear understanding of the invention, one embodiment of the lastmentioned overall arrangement is illustrated, partly in diagrammatic form and partly in circuit diagram form, in the accompanying drawing. This embodiment has been successfully tested in animal trials with a baboon and is considered applicable to man.
DETAILED DESCRIPTION OF A PRESENTL PREFERRED EMBODIMENT The illustrated embodiment is in two parts denoted at 10 and 11 of which the first is implantable and the second employed externally of the body. Also these two parts 10 and 11 are themselves functionally subdivided into portions 10A, 10B and 11A, 118, although thissubdivision does not necessarily involve physical separation.
The implantable portion A is the circuit which provides the hold mode of control referred to above and comprises a complementary multivibrator stage operable to generate a pulse train of twenty pulses per second which are applied through a buffer stage 21 and output stage 22 to stimulating electrodes 23A. The electrodes 23A are located adjacent the relevant ventralsacral roots by use of electrode terminal devices such as describedin US. Pat. No. 3,718,134 and the tissue load at the electrodes is denoted by broken line resistor RlA; This circuit is powered by a mercury cell 24, resistor R2 in the multivibrator stage is chosen so that fifty microsecond pulses are generated, and the potentiometer R3 affords adjustment of the output pulse intensity to a low level at which only the sphincter mus cle is contracted. Potentiometer R3 is preferably ad- 'justable post-operatively from without the body and this can be effected by use of a magnetic coupling.
The remaining components of the relevant circuit constitute an inhibiting stage 25 in the form of a simple radio receiver which is actuated in response to the external portion 11A to hold the multivibrator transistor switched off.
The implantable portion 108 is also of simple radio receiver form and serves, in response to the external portion 11B, to energise further stimulating electrodes 238, in response to the external portion 11B.
As will be apparent from the above discussion, the external portions 11A, 11B are radio transmitters and it is unnecessary to consider more detailed circuit design since these portions can be of any suitable form to serve the relevant function requirements.
The more complex of these requirements is for the portion 118 which as mentioned earlier is to provide a relatively high intensity, interrupted pulse train signal. In the development in question the portion 118 comprised two multivibrators connected in cascade, with the first activating the second for a period of 120 milliseconds each 1 /2 seconds, the second generating 12 /2 millisecond pulses at 9 /2 milliseconds separation during each period of activation, and the last-mentioned pulses gating the radio frequency output of the relevant transmitter.
The more simple requirement is for the portion 11A which is operated at the same time as portion 118 to provide a radio signal .to inhibit the portion 10A.
Component values in the illustrated circuits are as follows:
While the invention has been described, and indeed developed so far, with reference to urinarycontrol in respect of disorders of neurological origin, the invention may afford similar control in respect of disorders of non-neurological origin, such as urinary incontinence arising from gynaecological defects. By the same token, it will be appreciated that use of both of the above-discussed more specific modes of control is not essential in all applications of the invention.
We claim:
l. A method of urinary control which comprises applying an electricalsignal of continuous pulse train form to'the sacralventral roots,.said sacral ventral roots communicating with the sphincter muscle and bladder muscle, thereby causing the step of contracting said sphincter muscle while said bladder muscle is relaxed. i i
2. A method according to claim 1 wherein said pulse 3 train has a pulse repetition rate of about 20 per second.
3. A method of urinary control which comprises applying an electrical signal of interrupted pulse train form'to the sacral ventral roots, said sacral ventral roots communicating with the sphincter muscle and bladder muscle, thereby causing the step of contracting both of said muscles during each pulse train and the further step of maintaining said bladder muscle contracted during part of each interruption period between successive pulse trains when said sphincter muscle is relaxed.
4. A method according to claim 3 wherein said pulse trains are of short duration during successive intervals of about 1 /2 seconds, and each comprise about twelve pulses.
5. A method according to claim 4 wherein each of said pulse trains comprises pulses of about /2 millisecond duration each 10 milliseconds.
6. A method of urinary control which comprises alternatively applying two different pulsatile electrical signals to the sacral ventral roots, said sacral ventral roots communicating with the sphincter muscle and bladder muscle to thereby cause the step of stimulating said muscles, one of said signals being of lower intensity and higher repetition rate for causing the step of contracting said sphincter muscle while said bladder muscle is relaxed, and the other signal being of higher intensity and lower repetition rate for causing the step of contraction of both of said muscles during each pulse and to cause the further step of maintaining said bladder muscle contracted during part of successive interpulse periods when said sphincter muscle is relaxed.
7. A method of urinary control in primates, comprising:
applying pulsing electrical signals to the sacral ventral roots which control contraction of the detrusor muscle for the bladder and the striated, sphincter muscles which contribute to closing the urethra, in two different modes;
in the first of which, the signals are of a first intensity for the step of contracting the urethra closing muscles, but not contracting the bladder detrusor muscle, and including the step of spacing the first intensity pulses such that the urethra closing muscles do not become substantially relaxed between pulses; and
in the second of which, the signals are of a second intensity higher than said first intensity signals for causing the step of contracting both the urethra closing muscles and the bladder detrusor muscle,
' and including the step of spacing the second intensity pulses such that the urethra closing muscles, but not the bladder detrusor muscle become relaxed between pulses, such that pressure exerted on the bladder by the detrusor muscle in between pulses when the urethra closing muscles have relaxed, forces urine from the bladder and out through the urethra.
8. The method of claim 7, wherein the applying step comprises:
implanting in the subject primate:
a. electrode means disposed for stimulating the third and fourth, left and right sacral ventral motor nerve fibre roots, without substantially stimulating sensory nerve fibres;
b. multivibrator means and an electrical power supply therefor, for emitting said first intensity signals and a connection for communicating these signals to said electrode means;
c. inhibiting means for preventing communication of said first intensity signals to said electrode means upon command;
d. receiver means for receiving a command signal from outside the subject primate and connected to the inhibiting means for commanding same;
e. multivibrator means for emitting said second intensity signals and a connection for communicating these signals to said electrode means;
f. receiver means for receiving a command signal from outside the subject primate and connected to the multivibrator means to emit said second intensity signals;
wherein changing modes from the first to the second comprises: sending command signals from outside the subject primate to the receiver means of (d) and to the receiver means of (f); and
wherein changing modes from the second to the first comprises: terminating the sending of said command signals from outside the subject primate.
9. The method of claim 8, wherein: the implanted multivibrator means of (b) includes electrical output intensity adjustment means and the method further comprises: post operatively adjusting the intensity of signals provided by the implanted multivibrator means of (b) by adjusting the intensity adjustment means to ensure desired first mode operation wherein there occurs contraction of the striated, sphincter muscles which contribute to closing the urethra without substantially contracting the bladder detrusor muscle.
10. Urinary control apparatus comprising:
a. stimulating electrode devices adapted for connection to the sacral ventral roots;
b. a first electrical circuit means operable to generate a low intensity, continuous pulse train signal, which circuit means is connected to said electrode devices to energize the same;
c. a second electrical circuit means operable to generate a high intensity, interrupted pulse train signal, which circuit means is connected to said electrode devices to energize the same; and
d. means for alternatively activating said first and second circuit means to energize said electrode devices;
e. said electrode devices and at least part of both said first and second circuit means being adapted for bodily implantation, and at least part of said activating means being for use outside the body.
11. Urinary control apparatus comprising:
a, stimulating electrode devices adapted for connection to the sacral ventral roots;
b. an implantable electric circuit means, including a power source, operable to generate a low intensity continuous pulse train signal, which circuit means is connected to said electrode devices to energize the same;
c. radio transmitter means for use outside the body operable to generate a first signal including at least a high intensity interrupted pulse train and a second signal;
d. an implantable first radio receiver means operable in response to said interrupted pulse train and connected to said electrode devices to energize the same; and
e. an implantable second radio receiver means operable in response to said second signal and connected to said electric circuit to inhibit operation of the same.
12. Apparatus for effecting urinary control in primates by applying pulsing electrical signals to the sacral ventral roots which control contraction of the detrusor muscle for the bladder and the striated, sphincter muscles which contribute to closing the urethra, in two different modes;
in the first of which, the signals are of a low intensity so as to contract the urethra closing muscles, but not to contract the bladder detrusor muscle, and wherein these low intensity signals are of such spacing between pulses that the urethra closing muscles do not become substantially relaxed between pulses; and
in the second of which, the signals are of a different intensity higher than said low intensity signals so as to contract both the urethra closing muscles and the bladder detrusor muscle, but of such spacing between pulses, that the urethra closing muscles, but not the bladder detrusor muscle become sufficiently relaxed between pulses, that pressure exerted on the bladder by the detrusor muscle in between pulses when the urethra closing muscles have relaxed, forces urine from the bladder and out through the urethra;
said apparatus comprising a surgical implant which includes:
a. electrode means being disposed, when implanted,
to stimulate the third and fourth, left and right sacral ventral motor nerve fibre roots, without substantially stimulating sensory nerve fibres;
b. multivibrator means including an electrical power supply therefor, for emitting said low intensity signals and a connection for communicating these signals to said electrode means;
0. inhibiting means for preventing communication of said low intensity signals to said electrode means upon the occurrence of a first command signal;
d. receiver means for receiving the first command signal from outside the subject primate and connected to the inhibiting means for controlling same;
e. multivibrator means for emitting said higher intensity signals and a connection for communicating these signals to said electrode means;
f. receiver means for receiving a second command signal from outside the subject primate and connected to the multivibrator means of (e) for commanding and powering that multivibrator means to emit said higher intensity signals;
and said apparatus further comprising external transmitter means for sending said first and second command signals;
whereby, the sending of command signals from outside the subject primate to the receiver means of (d) and to the receiver means of (f) places urinary control in the second mode thereof and terminating the sending of said command signals places urinary control in the first mode thereof.

Claims (12)

1. A method of urinary control which comprises applying an electrical signal of continuous pulse train form to the sacral ventral roots, said sacral ventral roots communicating with the sphincter muscle and bladder muscle, thereby causing the step of contracting said sphincter muscle while said bladder muscle is relaxed.
1. A method of urinary control which comprises applying an electrical signal of continuous pulse train form to the sacral ventral roots, said sacral ventral roots communicating with the sphincter muscle and bladder muscle, thereby causing the step of contracting said sphincter muscle while said bladder muscle is relaxed.
2. A method according to claim 1 wherein said pulse train has a pulse repetition rate of about 20 per second.
3. A method of urinary control which comprises applying an electrical signal of interrupted pulse train form to the sacral ventral roots, said sacral ventral roots communicating with the sphincter muscle and bladder muscle, thereby causing the step of contracting both of said muscles during each pulse train and the further step of maintaining said bladder muscle contracted during part of each interruption period between successive pulse trains when said sphincter muscle is relaxed.
4. A method according to claim 3 wherein said pulse trains are of short duration during successive intervals of about 1 1/2 seconds, and each comprise about twelve pulses.
5. A method according to claim 4 wherein each of said pulse trains comprises pulses of about 1/2 millisecond duration each 10 milliseconds.
6. A method of urinary control which comprises alternatively applying two different pulsatile electrical signals to the sacral ventral roots, said sacral ventral roots communicating with the sphincter muscle and bladder muscle to thereby cause the step of stimulating said muscles, one of said signals being of lower intensity and higher repetition rate for causing the step of contracting said sphincter muscle while said bladder muscle is relaxed, and the other signal being of higher intensity and lower repetition rate for causing the step of contraction of both of said muscles during each pulse and to cause the further step of maintaining said bladder muscle contracted during part of successive inter-pulse periods when said sphincter muscle is relaxed.
7. A method of urinary control in primates, comprising: applying pulsing electrical signals to the sacral ventral roots which control contraction of the detrusor muscle for the bladder and the striated, sphincter muscles which contribute to closing the urethra, in two different modes; in the first of which, the signals are of a first intensity for the step of contracting the urethra closing muscles, but not contracting the bladder detrusor muscle, and including the step of spacing the first intensity pulses such that the urethra closing muscles do not become substantially relaxed between pulses; and in the second of which, the signals are of a second intensity higher than said first intensity signals for causing the step of contracting both the urethra closing muscles and the bladder detrusor muscle, and including the step of spacing the second intensity pulses such that the urethra closing muscles, but not the bladder detrusor muscle become relaxed between pulses, such that pressure exerted on the bladder by the detrusor muscle in between pulses when the urethra closing muscles have relaxed, forces urine from the bladder and out through the urethra.
8. The method of claim 7, wherein the applying step comprises: implanting in the subject primate: a. electrode means disposed for stimulating the third and fourth, left and right sacral ventral motor nerve fibre roots, without substantially stimulating sensory nerve fibres; b. multivibrator means and an electrical power supply therefor, for emitting said first intensity signals and a connection for communicating these signals to said electrode means; c. inhibiting means for preventing communication of said first intensity signals to said electrode means upon command; d. receiver means for receiving a command signal from outside the subject primate and connected to the inhibiting means for commanding same; e. multivibrator means for emitting said second intensity signals and a connection for communicating these signals to said electrode means; f. receiver means for receiving a command signal from outside the subject primate and connected to the multivibrator means to emit said second intensity signals; wherein changing modes from the first to the second comprises: sending command signals from outside the subject primate to the receiver means of (d) and to the receiver means of (f); and wherein changing modes from the second to the first comprises: terminating the sending of said command signals from outside the subject primate.
9. The method of claim 8, wherein: the implanted multivibrator means of (b) includes electrical output intensity adjustment means and the method further comprises: post operatively adjusting the intensity of signals provided by the implanted multivibrator means of (b) by adjusting the intensity adjustment means to ensure desired first mode operation wherein thEre occurs contraction of the striated, sphincter muscles which contribute to closing the urethra without substantially contracting the bladder detrusor muscle.
10. Urinary control apparatus comprising: a. stimulating electrode devices adapted for connection to the sacral ventral roots; b. a first electrical circuit means operable to generate a low intensity, continuous pulse train signal, which circuit means is connected to said electrode devices to energize the same; c. a second electrical circuit means operable to generate a high intensity, interrupted pulse train signal, which circuit means is connected to said electrode devices to energize the same; and d. means for alternatively activating said first and second circuit means to energize said electrode devices; e. said electrode devices and at least part of both said first and second circuit means being adapted for bodily implantation, and at least part of said activating means being for use outside the body.
11. Urinary control apparatus comprising: a. stimulating electrode devices adapted for connection to the sacral ventral roots; b. an implantable electric circuit means, including a power source, operable to generate a low intensity continuous pulse train signal, which circuit means is connected to said electrode devices to energize the same; c. radio transmitter means for use outside the body operable to generate a first signal including at least a high intensity interrupted pulse train and a second signal; d. an implantable first radio receiver means operable in response to said interrupted pulse train and connected to said electrode devices to energize the same; and e. an implantable second radio receiver means operable in response to said second signal and connected to said electric circuit to inhibit operation of the same.
US354910A 1972-04-27 1973-04-26 Urinary control Expired - Lifetime US3870051A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1958372A GB1434524A (en) 1972-04-27 1972-04-27 Urinary control apparatus

Publications (1)

Publication Number Publication Date
US3870051A true US3870051A (en) 1975-03-11

Family

ID=10131805

Family Applications (1)

Application Number Title Priority Date Filing Date
US354910A Expired - Lifetime US3870051A (en) 1972-04-27 1973-04-26 Urinary control

Country Status (2)

Country Link
US (1) US3870051A (en)
GB (1) GB1434524A (en)

Cited By (109)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2493074A1 (en) * 1980-10-23 1982-04-30 Gorenje Tovarna Gospodinjske CONTROL CIRCUIT FOR A THERAPEUTIC STIMULATOR FOR TREATMENT OF URINARY INCONTINENCE
WO1982001656A1 (en) * 1980-11-20 1982-05-27 Roy E Mcdonnell Electrical control of body discharges and headaches
US4569351A (en) * 1984-12-20 1986-02-11 University Of Health Sciences/The Chicago Medical School Apparatus and method for stimulating micturition and certain muscles in paraplegic mammals
US4585005A (en) * 1984-04-06 1986-04-29 Regents Of University Of California Method and pacemaker for stimulating penile erection
EP0245547A1 (en) * 1986-05-12 1987-11-19 The Regents Of The University Of California Electronic control system for controlling pelvic viscera via neuro-electrical stimulation
US4742833A (en) * 1985-01-03 1988-05-10 Richard Wolf Gmbh Device for treating male persons suffering from urine incontinence
US4785828A (en) * 1986-10-06 1988-11-22 Empi, Inc. Vaginal stimulator for controlling urinary incontinence in women
US4873996A (en) * 1986-10-06 1989-10-17 Empi, Inc. Vaginal stimulator for controlling urinary incontinence in women
US4881526A (en) * 1988-05-27 1989-11-21 Empi, Inc. Intravaginal electrode and stimulation system for controlling female urinary incontinence
US5193539A (en) * 1991-12-18 1993-03-16 Alfred E. Mann Foundation For Scientific Research Implantable microstimulator
US5193540A (en) * 1991-12-18 1993-03-16 Alfred E. Mann Foundation For Scientific Research Structure and method of manufacture of an implantable microstimulator
US5199430A (en) * 1991-03-11 1993-04-06 Case Western Reserve University Micturitional assist device
US5291902A (en) * 1993-01-11 1994-03-08 Brent Carman Incontinence treatment
US5454840A (en) * 1994-04-05 1995-10-03 Krakovsky; Alexander A. Potency package
US5562717A (en) * 1992-05-23 1996-10-08 Axelgaard Manufacturing Company, Ltd. Electrical stimulation for treatment of incontinence and other neuromuscular disorders
WO2000015293A1 (en) * 1998-09-16 2000-03-23 Axon Engineering, Inc. Combined stimulation of ventral and dorsal sacral roots for control of bladder function
US6061596A (en) * 1995-11-24 2000-05-09 Advanced Bionics Corporation Method for conditioning pelvic musculature using an implanted microstimulator
WO2001089629A1 (en) * 2000-05-26 2001-11-29 Consejo Superior De Investigaciones Científicas Sacral root stimulating system by means of a radio-frequency powered implant
WO2001089630A1 (en) * 2000-05-26 2001-11-29 Consejo Superior De Investigaciones Científicas Urination, defecation and erection control system in neuropathy patients
US6354991B1 (en) 1998-10-06 2002-03-12 Bio Control Medical Ltd Incontinence treatment device
WO2002047760A1 (en) 2000-12-12 2002-06-20 Universite De Sherbrooke Implantable neurostimulator
US6505074B2 (en) * 1998-10-26 2003-01-07 Birinder R. Boveja Method and apparatus for electrical stimulation adjunct (add-on) treatment of urinary incontinence and urological disorders using an external stimulator
US20030018365A1 (en) * 2001-07-20 2003-01-23 Loeb Gerald E. Method and apparatus for the treatment of urinary tract dysfunction
US20030082884A1 (en) * 2001-10-26 2003-05-01 International Business Machine Corporation And Kabushiki Kaisha Toshiba Method of forming low-leakage dielectric layer
US6615085B1 (en) * 1998-10-26 2003-09-02 Birinder R. Boveja Apparatus for adjunct (add-on) therapy of Dementia and Alzheimer's disease utilizing an implantable lead and an external stimulator
US6659936B1 (en) 1999-08-04 2003-12-09 University Of Melbourne Method and apparatus for treating incontinence
US6712772B2 (en) 2001-11-29 2004-03-30 Biocontrol Medical Ltd. Low power consumption implantable pressure sensor
US6735474B1 (en) 1998-07-06 2004-05-11 Advanced Bionics Corporation Implantable stimulator system and method for treatment of incontinence and pain
US6836684B1 (en) 1998-10-30 2004-12-28 Neurocon Aps Method to control an overactive bladder
US6862480B2 (en) 2001-11-29 2005-03-01 Biocontrol Medical Ltd. Pelvic disorder treatment device
US20050055063A1 (en) * 2001-07-20 2005-03-10 Loeb Gerald E. Method and apparatus for the treatment of urinary tract dysfunction
US20050060005A1 (en) * 2001-03-30 2005-03-17 Case Western Reserve University Systems and methods for stimulating components in, on, or near the pudendal nerve or its branches to achieve selective physiologic responses
US6896651B2 (en) 1998-10-06 2005-05-24 Biocontrol Medical Ltd. Mechanical and electrical sensing for incontinence treatment
US6907293B2 (en) 2001-03-30 2005-06-14 Case Western Reserve University Systems and methods for selectively stimulating components in, on, or near the pudendal nerve or its branches to achieve selective physiologic responses
US20050143783A1 (en) * 2003-05-11 2005-06-30 Boveja Birinder R. Method and system for providing pulsed electrical stimulation to sacral plexus of a patient to provide therapy for urinary incontinence and urological disorders
US6941171B2 (en) 1998-07-06 2005-09-06 Advanced Bionics Corporation Implantable stimulator methods for treatment of incontinence and pain
US20050216069A1 (en) * 2001-11-29 2005-09-29 Biocontrol Medical Ltd. Pelvic disorder treatment device
US20050228451A1 (en) * 1998-07-06 2005-10-13 Jaax Kristen N Methods and systems for treating chronic pelvic pain
US20050251212A1 (en) * 2000-09-27 2005-11-10 Cvrx, Inc. Stimulus regimens for cardiovascular reflex control
US20050278000A1 (en) * 2004-06-10 2005-12-15 Strother Robert B Implantable pulse generator for providing functional and/or therapeutic stimulation of muscles and/or nerves and/or central nervous system tissue
US20050288729A1 (en) * 2004-06-08 2005-12-29 Imad Libbus Coordinated therapy for disordered breathing including baroreflex modulation
US20060004421A1 (en) * 2004-02-12 2006-01-05 Bennett Maria E Systems and methods for bilateral stimulation of left and right branches of the dorsal genital nerves to treat dysfunctions, such as urinary incontinence
US20060111626A1 (en) * 2003-03-27 2006-05-25 Cvrx, Inc. Electrode structures having anti-inflammatory properties and methods of use
US7054689B1 (en) 2000-08-18 2006-05-30 Advanced Bionics Corporation Fully implantable neurostimulator for autonomic nerve fiber stimulation as a therapy for urinary and bowel dysfunction
US7062330B1 (en) * 1998-10-26 2006-06-13 Boveja Birinder R Electrical stimulation adjunct (Add-ON) therapy for urinary incontinence and urological disorders using implanted lead stimulus-receiver and an external pulse generator
US7142925B1 (en) * 1998-09-16 2006-11-28 Axon Engineering, Inc. Combined stimulation of ventral and dorsal sacral roots for control of bladder function
US20070021792A1 (en) * 2000-09-27 2007-01-25 Cvrx, Inc. Baroreflex Modulation Based On Monitored Cardiovascular Parameter
US20070038259A1 (en) * 2000-09-27 2007-02-15 Cvrx, Inc. Method and apparatus for stimulation of baroreceptors in pulmonary artery
US20070060980A1 (en) * 2004-06-10 2007-03-15 Ndi Medical, Llc Implantable pulse generator systems and methods for providing functional and/or therapeutic stimulation of muscles and/or nerves and/or central nervous system tissue
US20070060968A1 (en) * 2004-06-10 2007-03-15 Ndi Medical, Llc Implantable pulse generator systems and methods for providing functional and/or therapeutic stimulation of muscles and/or nerves and/or central nervous system tissue
US20070066995A1 (en) * 2004-06-10 2007-03-22 Ndi Medical, Llc Implantable pulse generator systems and methods for providing functional and/or therapeutic stimulation of muscles and/or nerves and/or central nervous system tissue
US20070088397A1 (en) * 2005-10-14 2007-04-19 Jacobson Peter M Leadless cardiac pacemaker system with conductive communication
US20070161873A1 (en) * 2002-12-04 2007-07-12 Cardiac Pacemakers, Inc. Sleep detection using an adjustable threshold
US20070161912A1 (en) * 2006-01-10 2007-07-12 Yunlong Zhang Assessing autonomic activity using baroreflex analysis
US20070185543A1 (en) * 2000-09-27 2007-08-09 Cvrx, Inc. System and method for sustained baroreflex stimulation
US20070260288A1 (en) * 2006-03-03 2007-11-08 Yossi Gross Apparatus for treating stress and urge incontinence
US20070265675A1 (en) * 2006-05-09 2007-11-15 Ams Research Corporation Testing Efficacy of Therapeutic Mechanical or Electrical Nerve or Muscle Stimulation
US20070293910A1 (en) * 2004-06-10 2007-12-20 Ndi Medical, Inc. Implantable pulse generator for providing functional and/or therapeutic stimulation of muscles and/or nerves and/or central nervous system tissue
US20080009914A1 (en) * 2006-07-10 2008-01-10 Ams Research Corporation Systems and Methods for Implanting Tissue Stimulation Electrodes in the Pelvic Region
US7343202B2 (en) 2004-02-12 2008-03-11 Ndi Medical, Llc. Method for affecting urinary function with electrode implantation in adipose tissue
US20080161874A1 (en) * 2004-02-12 2008-07-03 Ndi Medical, Inc. Systems and methods for a trial stage and/or long-term treatment of disorders of the body using neurostimulation
US20080161876A1 (en) * 2006-12-21 2008-07-03 Ams Research Corporation Electrode implantation in male external urinary sphincter
US20080171923A1 (en) * 2000-09-27 2008-07-17 Cvrx, Inc. Assessing autonomic activity using baroreflex analysis
US20090012592A1 (en) * 2006-07-10 2009-01-08 Ams Research Corporation Tissue anchor
US20090082828A1 (en) * 2007-09-20 2009-03-26 Alan Ostroff Leadless Cardiac Pacemaker with Secondary Fixation Capability
US20090157091A1 (en) * 2006-04-04 2009-06-18 Ams Research Corporation Apparatus for Implanting Neural Stimulation Leads
US20090234418A1 (en) * 2000-09-27 2009-09-17 Kieval Robert S Devices and methods for cardiovascular reflex control via coupled electrodes
US20100049289A1 (en) * 2007-07-10 2010-02-25 Ams Research Corporation Tissue anchor
US20100076254A1 (en) * 2006-06-05 2010-03-25 Ams Research Corporation Electrical muscle stimulation to treat fecal incontinence and/or pelvic prolapse
US7747323B2 (en) 2004-06-08 2010-06-29 Cardiac Pacemakers, Inc. Adaptive baroreflex stimulation therapy for disordered breathing
US7761167B2 (en) 2004-06-10 2010-07-20 Medtronic Urinary Solutions, Inc. Systems and methods for clinician control of stimulation systems
US20100198288A1 (en) * 2009-02-02 2010-08-05 Alan Ostroff Leadless Cardiac Pacemaker with Secondary Fixation Capability
US20100217340A1 (en) * 2009-02-23 2010-08-26 Ams Research Corporation Implantable Medical Device Connector System
US20100249874A1 (en) * 2000-09-27 2010-09-30 Bolea Stephen L Baroreflex therapy for disordered breathing
US20110077708A1 (en) * 2009-09-28 2011-03-31 Alan Ostroff MRI Compatible Leadless Cardiac Pacemaker
US20110160793A1 (en) * 2009-12-31 2011-06-30 Ams Research Corporation Multi-Zone Stimulation Implant System and Method
US8195304B2 (en) 2004-06-10 2012-06-05 Medtronic Urinary Solutions, Inc. Implantable systems and methods for acquisition and processing of electrical signals
US8467875B2 (en) 2004-02-12 2013-06-18 Medtronic, Inc. Stimulation of dorsal genital nerves to treat urologic dysfunctions
US8543205B2 (en) 2010-10-12 2013-09-24 Nanostim, Inc. Temperature sensor for a leadless cardiac pacemaker
US8577467B2 (en) 2011-09-30 2013-11-05 Nyxoah SA Apparatus and method for controlling energy delivery as a function of degree of coupling
US8594794B2 (en) 2007-07-24 2013-11-26 Cvrx, Inc. Baroreflex activation therapy with incrementally changing intensity
US8606356B2 (en) 2003-09-18 2013-12-10 Cardiac Pacemakers, Inc. Autonomic arousal detection system and method
US8615310B2 (en) 2010-12-13 2013-12-24 Pacesetter, Inc. Delivery catheter systems and methods
US9020611B2 (en) 2010-10-13 2015-04-28 Pacesetter, Inc. Leadless cardiac pacemaker with anti-unscrewing feature
US9060692B2 (en) 2010-10-12 2015-06-23 Pacesetter, Inc. Temperature sensor for a leadless cardiac pacemaker
US9126032B2 (en) 2010-12-13 2015-09-08 Pacesetter, Inc. Pacemaker retrieval systems and methods
US9168383B2 (en) 2005-10-14 2015-10-27 Pacesetter, Inc. Leadless cardiac pacemaker with conducted communication
US9220887B2 (en) 2011-06-09 2015-12-29 Astora Women's Health LLC Electrode lead including a deployable tissue anchor
US9242102B2 (en) 2010-12-20 2016-01-26 Pacesetter, Inc. Leadless pacemaker with radial fixation mechanism
US9393411B2 (en) 2008-04-02 2016-07-19 Case Western Reserve University System and method of bladder and sphincter control
US9409013B2 (en) 2009-10-20 2016-08-09 Nyxoah SA Method for controlling energy delivery as a function of degree of coupling
US9415215B2 (en) 2009-10-20 2016-08-16 Nyxoah SA Methods for treatment of sleep apnea
US9427573B2 (en) 2007-07-10 2016-08-30 Astora Women's Health, Llc Deployable electrode lead anchor
US9452287B2 (en) 2013-01-21 2016-09-27 Cala Health, Inc. Devices and methods for controlling tremor
US9480846B2 (en) 2006-05-17 2016-11-01 Medtronic Urinary Solutions, Inc. Systems and methods for patient control of stimulation systems
US9511236B2 (en) 2011-11-04 2016-12-06 Pacesetter, Inc. Leadless cardiac pacemaker with integral battery and redundant welds
US9539433B1 (en) 2009-03-18 2017-01-10 Astora Women's Health, Llc Electrode implantation in a pelvic floor muscular structure
US9731112B2 (en) 2011-09-08 2017-08-15 Paul J. Gindele Implantable electrode assembly
US9802041B2 (en) 2014-06-02 2017-10-31 Cala Health, Inc. Systems for peripheral nerve stimulation to treat tremor
US9802054B2 (en) 2012-08-01 2017-10-31 Pacesetter, Inc. Biostimulator circuit with flying cell
US20180169409A1 (en) * 2016-12-21 2018-06-21 University Of Southern California Smooth muscle electrical stimulation based on entrainment of intracellular calcium ion oscillations
US10201702B2 (en) 2010-11-30 2019-02-12 Medtronic, Inc. Pelvic floor muscle training
US10765856B2 (en) 2015-06-10 2020-09-08 Cala Health, Inc. Systems and methods for peripheral nerve stimulation to treat tremor with detachable therapy and monitoring units
US10814130B2 (en) 2016-07-08 2020-10-27 Cala Health, Inc. Dry electrodes for transcutaneous nerve stimulation
US11331480B2 (en) 2017-04-03 2022-05-17 Cala Health, Inc. Systems, methods and devices for peripheral neuromodulation for treating diseases related to overactive bladder
US11344722B2 (en) 2016-01-21 2022-05-31 Cala Health, Inc. Systems, methods and devices for peripheral neuromodulation for treating diseases related to overactive bladder
US11596785B2 (en) 2015-09-23 2023-03-07 Cala Health, Inc. Systems and methods for peripheral nerve stimulation in the finger or hand to treat hand tremors
US11857778B2 (en) 2018-01-17 2024-01-02 Cala Health, Inc. Systems and methods for treating inflammatory bowel disease through peripheral nerve stimulation
US11890468B1 (en) 2019-10-03 2024-02-06 Cala Health, Inc. Neurostimulation systems with event pattern detection and classification

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3236240A (en) * 1962-09-06 1966-02-22 Univ Minnesota Implantable bladder stimulator
US3650276A (en) * 1969-03-26 1972-03-21 Inst Demedicina Si Farmacie Method and apparatus, including a flexible electrode, for the electric neurostimulation of the neurogenic bladder
US3667477A (en) * 1966-11-25 1972-06-06 Canadian Patents Dev Implantable vesical stimulator

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3236240A (en) * 1962-09-06 1966-02-22 Univ Minnesota Implantable bladder stimulator
US3667477A (en) * 1966-11-25 1972-06-06 Canadian Patents Dev Implantable vesical stimulator
US3650276A (en) * 1969-03-26 1972-03-21 Inst Demedicina Si Farmacie Method and apparatus, including a flexible electrode, for the electric neurostimulation of the neurogenic bladder

Cited By (282)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2493074A1 (en) * 1980-10-23 1982-04-30 Gorenje Tovarna Gospodinjske CONTROL CIRCUIT FOR A THERAPEUTIC STIMULATOR FOR TREATMENT OF URINARY INCONTINENCE
US4387719A (en) * 1980-10-23 1983-06-14 Gorenje Tovarna Gospodinjske Opreme N.Sol.O. Velenje Control circuit of a therapeutic stimulator for the urinary incontinence
WO1982001656A1 (en) * 1980-11-20 1982-05-27 Roy E Mcdonnell Electrical control of body discharges and headaches
US4537195A (en) * 1980-11-20 1985-08-27 Mcdonnell Roy E Electrical control of body discharges and headaches
US4585005A (en) * 1984-04-06 1986-04-29 Regents Of University Of California Method and pacemaker for stimulating penile erection
US4569351A (en) * 1984-12-20 1986-02-11 University Of Health Sciences/The Chicago Medical School Apparatus and method for stimulating micturition and certain muscles in paraplegic mammals
US4742833A (en) * 1985-01-03 1988-05-10 Richard Wolf Gmbh Device for treating male persons suffering from urine incontinence
EP0245547A1 (en) * 1986-05-12 1987-11-19 The Regents Of The University Of California Electronic control system for controlling pelvic viscera via neuro-electrical stimulation
US4785828A (en) * 1986-10-06 1988-11-22 Empi, Inc. Vaginal stimulator for controlling urinary incontinence in women
US4873996A (en) * 1986-10-06 1989-10-17 Empi, Inc. Vaginal stimulator for controlling urinary incontinence in women
US4881526A (en) * 1988-05-27 1989-11-21 Empi, Inc. Intravaginal electrode and stimulation system for controlling female urinary incontinence
US5199430A (en) * 1991-03-11 1993-04-06 Case Western Reserve University Micturitional assist device
US5193539A (en) * 1991-12-18 1993-03-16 Alfred E. Mann Foundation For Scientific Research Implantable microstimulator
US5193540A (en) * 1991-12-18 1993-03-16 Alfred E. Mann Foundation For Scientific Research Structure and method of manufacture of an implantable microstimulator
US5324316A (en) * 1991-12-18 1994-06-28 Alfred E. Mann Foundation For Scientific Research Implantable microstimulator
US5562717A (en) * 1992-05-23 1996-10-08 Axelgaard Manufacturing Company, Ltd. Electrical stimulation for treatment of incontinence and other neuromuscular disorders
US5291902A (en) * 1993-01-11 1994-03-08 Brent Carman Incontinence treatment
US5454840A (en) * 1994-04-05 1995-10-03 Krakovsky; Alexander A. Potency package
US6061596A (en) * 1995-11-24 2000-05-09 Advanced Bionics Corporation Method for conditioning pelvic musculature using an implanted microstimulator
US6735474B1 (en) 1998-07-06 2004-05-11 Advanced Bionics Corporation Implantable stimulator system and method for treatment of incontinence and pain
US6941171B2 (en) 1998-07-06 2005-09-06 Advanced Bionics Corporation Implantable stimulator methods for treatment of incontinence and pain
US7890176B2 (en) 1998-07-06 2011-02-15 Boston Scientific Neuromodulation Corporation Methods and systems for treating chronic pelvic pain
US20050228451A1 (en) * 1998-07-06 2005-10-13 Jaax Kristen N Methods and systems for treating chronic pelvic pain
WO2000015293A1 (en) * 1998-09-16 2000-03-23 Axon Engineering, Inc. Combined stimulation of ventral and dorsal sacral roots for control of bladder function
US7142925B1 (en) * 1998-09-16 2006-11-28 Axon Engineering, Inc. Combined stimulation of ventral and dorsal sacral roots for control of bladder function
US20080242918A1 (en) * 1998-10-06 2008-10-02 Ams Research Corporation Incontinence Treatment Device
US20050261746A1 (en) * 1998-10-06 2005-11-24 Yossi Gross Control of urge incontinence
US6354991B1 (en) 1998-10-06 2002-03-12 Bio Control Medical Ltd Incontinence treatment device
US8083663B2 (en) 1998-10-06 2011-12-27 Ams Research Corporation Pelvic disorder treatment
US7582053B2 (en) 1998-10-06 2009-09-01 Ams Research Corporation Control of urge incontinence
US8340786B2 (en) 1998-10-06 2012-12-25 Ams Research Corporation Incontinence treatment device
US6652449B1 (en) 1998-10-06 2003-11-25 Bio Control Medical, Ltd. Control of urge incontinence
US20050113881A1 (en) * 1998-10-06 2005-05-26 Yossi Gross Incontinence treatment device
US6896651B2 (en) 1998-10-06 2005-05-24 Biocontrol Medical Ltd. Mechanical and electrical sensing for incontinence treatment
US7387603B2 (en) 1998-10-06 2008-06-17 Ams Research Corporation Incontinence treatment device
US6505074B2 (en) * 1998-10-26 2003-01-07 Birinder R. Boveja Method and apparatus for electrical stimulation adjunct (add-on) treatment of urinary incontinence and urological disorders using an external stimulator
US6615085B1 (en) * 1998-10-26 2003-09-02 Birinder R. Boveja Apparatus for adjunct (add-on) therapy of Dementia and Alzheimer's disease utilizing an implantable lead and an external stimulator
US7062330B1 (en) * 1998-10-26 2006-06-13 Boveja Birinder R Electrical stimulation adjunct (Add-ON) therapy for urinary incontinence and urological disorders using implanted lead stimulus-receiver and an external pulse generator
US6836684B1 (en) 1998-10-30 2004-12-28 Neurocon Aps Method to control an overactive bladder
US6659936B1 (en) 1999-08-04 2003-12-09 University Of Melbourne Method and apparatus for treating incontinence
US20080195172A1 (en) * 1999-08-04 2008-08-14 The University Of Melbourne Method and apparatus for treating incontinence
US7384390B2 (en) 1999-08-04 2008-06-10 The University Of Melbourne Method and apparatus for treating incontinence
US20050119710A1 (en) * 1999-08-04 2005-06-02 Furness John B. Method and apparatus for treating incontinence
ES2161648A1 (en) * 2000-05-26 2001-12-01 Consejo Superior Investigacion Urination, defecation and erection control system in neuropathy patients
WO2001089630A1 (en) * 2000-05-26 2001-11-29 Consejo Superior De Investigaciones Científicas Urination, defecation and erection control system in neuropathy patients
WO2001089629A1 (en) * 2000-05-26 2001-11-29 Consejo Superior De Investigaciones Científicas Sacral root stimulating system by means of a radio-frequency powered implant
ES2164017A2 (en) * 2000-05-26 2002-02-01 Consejo Superior Investigacion Sacral root stimulating system by means of a radio-frequency powered implant
US8214048B1 (en) * 2000-08-18 2012-07-03 Boston Scientific Neuromodulation Corporation Fully implantable neurostimulator for autonomic nerve fiber stimulation as a therapy for urinary and bowel dysfunction
US8588917B2 (en) 2000-08-18 2013-11-19 Boston Scientific Neuromodulation Corporation Fully implantable neurostimulator for autonomic nerve fiber stimulation as a therapy for urinary and bowel dysfunction
US7054689B1 (en) 2000-08-18 2006-05-30 Advanced Bionics Corporation Fully implantable neurostimulator for autonomic nerve fiber stimulation as a therapy for urinary and bowel dysfunction
US20070167984A1 (en) * 2000-09-27 2007-07-19 Cvrx, Inc. Method and apparatus for stimulation of baroreceptors
US8606359B2 (en) 2000-09-27 2013-12-10 Cvrx, Inc. System and method for sustained baroreflex stimulation
US20050251212A1 (en) * 2000-09-27 2005-11-10 Cvrx, Inc. Stimulus regimens for cardiovascular reflex control
US20080215111A1 (en) * 2000-09-27 2008-09-04 Cvrx, Inc. Devices and Methods for Cardiovascular Reflex Control
US7949400B2 (en) 2000-09-27 2011-05-24 Cvrx, Inc. Devices and methods for cardiovascular reflex control via coupled electrodes
US8583236B2 (en) 2000-09-27 2013-11-12 Cvrx, Inc. Devices and methods for cardiovascular reflex control
US8290595B2 (en) 2000-09-27 2012-10-16 Cvrx, Inc. Method and apparatus for stimulation of baroreceptors in pulmonary artery
US20080177349A1 (en) * 2000-09-27 2008-07-24 Cvrx, Inc. Apparatus and method for modulating the baroreflex system
US20080172101A1 (en) * 2000-09-27 2008-07-17 Cvrx, Inc. Non-linear electrode array
US20080171923A1 (en) * 2000-09-27 2008-07-17 Cvrx, Inc. Assessing autonomic activity using baroreflex analysis
US8060206B2 (en) 2000-09-27 2011-11-15 Cvrx, Inc. Baroreflex modulation to gradually decrease blood pressure
US7840271B2 (en) 2000-09-27 2010-11-23 Cvrx, Inc. Stimulus regimens for cardiovascular reflex control
US9044609B2 (en) 2000-09-27 2015-06-02 Cvrx, Inc. Electrode structures and methods for their use in cardiovascular reflex control
US20070021792A1 (en) * 2000-09-27 2007-01-25 Cvrx, Inc. Baroreflex Modulation Based On Monitored Cardiovascular Parameter
US20070021799A1 (en) * 2000-09-27 2007-01-25 Cvrx, Inc. Automatic baroreflex modulation based on cardiac activity
US20070021796A1 (en) * 2000-09-27 2007-01-25 Cvrx, Inc. Baroreflex modulation to gradually decrease blood pressure
US20070021794A1 (en) * 2000-09-27 2007-01-25 Cvrx, Inc. Baroreflex Therapy for Disordered Breathing
US20070021797A1 (en) * 2000-09-27 2007-01-25 Cvrx, Inc. Baroreflex stimulation synchronized to circadian rhythm
US7813812B2 (en) 2000-09-27 2010-10-12 Cvrx, Inc. Baroreflex stimulator with integrated pressure sensor
US20070038259A1 (en) * 2000-09-27 2007-02-15 Cvrx, Inc. Method and apparatus for stimulation of baroreceptors in pulmonary artery
US20070038262A1 (en) * 2000-09-27 2007-02-15 Cvrx, Inc. Baroreflex stimulation system to reduce hypertension
US20070038261A1 (en) * 2000-09-27 2007-02-15 Cvrx, Inc. Lead for stimulating the baroreceptors in the pulmonary artery
US20070060972A1 (en) * 2000-09-27 2007-03-15 Cvrx, Inc. Devices and methods for cardiovascular reflex treatments
US20100249874A1 (en) * 2000-09-27 2010-09-30 Bolea Stephen L Baroreflex therapy for disordered breathing
US7801614B2 (en) 2000-09-27 2010-09-21 Cvrx, Inc. Stimulus regimens for cardiovascular reflex control
US8880190B2 (en) 2000-09-27 2014-11-04 Cvrx, Inc. Electrode structures and methods for their use in cardiovascular reflex control
US20100191303A1 (en) * 2000-09-27 2010-07-29 Cvrx, Inc. Automatic baroreflex modulation responsive to adverse event
US20100179614A1 (en) * 2000-09-27 2010-07-15 Kieval Robert S Devices and methods for cardiovascular reflex control
US20100174347A1 (en) * 2000-09-27 2010-07-08 Kieval Robert S Devices and methods for cardiovascular reflex control via coupled electrodes
US8712531B2 (en) 2000-09-27 2014-04-29 Cvrx, Inc. Automatic baroreflex modulation responsive to adverse event
US8838246B2 (en) 2000-09-27 2014-09-16 Cvrx, Inc. Devices and methods for cardiovascular reflex treatments
US8718789B2 (en) 2000-09-27 2014-05-06 Cvrx, Inc. Electrode structures and methods for their use in cardiovascular reflex control
US20090234418A1 (en) * 2000-09-27 2009-09-17 Kieval Robert S Devices and methods for cardiovascular reflex control via coupled electrodes
US9427583B2 (en) 2000-09-27 2016-08-30 Cvrx, Inc. Electrode structures and methods for their use in cardiovascular reflex control
US8086314B1 (en) * 2000-09-27 2011-12-27 Cvrx, Inc. Devices and methods for cardiovascular reflex control
US20070185543A1 (en) * 2000-09-27 2007-08-09 Cvrx, Inc. System and method for sustained baroreflex stimulation
US7623926B2 (en) 2000-09-27 2009-11-24 Cvrx, Inc. Stimulus regimens for cardiovascular reflex control
US20040102820A1 (en) * 2000-12-12 2004-05-27 Mouine Jaouhar Implantable neurostimulator
WO2002047760A1 (en) 2000-12-12 2002-06-20 Universite De Sherbrooke Implantable neurostimulator
US9446245B2 (en) 2001-03-30 2016-09-20 Case Western Reserve University Systems and methods for selectively stimulating components in, on, or near the pudendal nerve or its branches to achieve selectively physiological responses
US7623925B2 (en) 2001-03-30 2009-11-24 Case Western Reserve University Methods for selectively stimulating components in, on, or near the pudendal nerve or its branches to achieve selective physiologic responses
US6907293B2 (en) 2001-03-30 2005-06-14 Case Western Reserve University Systems and methods for selectively stimulating components in, on, or near the pudendal nerve or its branches to achieve selective physiologic responses
US7047078B2 (en) * 2001-03-30 2006-05-16 Case Western Reserve University Methods for stimulating components in, on, or near the pudendal nerve or its branches to achieve selective physiologic responses
US20050222636A1 (en) * 2001-03-30 2005-10-06 Case Western Reserve University Systems and methods for selectively stimulating components in, on, or near the pudendal nerve or its branches to achieve selective physiologic responses
US20050060005A1 (en) * 2001-03-30 2005-03-17 Case Western Reserve University Systems and methods for stimulating components in, on, or near the pudendal nerve or its branches to achieve selective physiologic responses
US20050055063A1 (en) * 2001-07-20 2005-03-10 Loeb Gerald E. Method and apparatus for the treatment of urinary tract dysfunction
US20030018365A1 (en) * 2001-07-20 2003-01-23 Loeb Gerald E. Method and apparatus for the treatment of urinary tract dysfunction
WO2003007885A3 (en) * 2001-07-20 2003-04-10 Alfred E Mann Inst Biomed Eng Method and apparatus for the treatment of urinary tract dysfunction
US20080097540A1 (en) * 2001-09-26 2008-04-24 Cvrx, Inc. Ecg input to implantable pulse generator using carotid sinus leads
US20070106340A1 (en) * 2001-09-26 2007-05-10 Cvrx, Inc. Electrode structures and methods for their use in cardiovascular reflex control
US20030082884A1 (en) * 2001-10-26 2003-05-01 International Business Machine Corporation And Kabushiki Kaisha Toshiba Method of forming low-leakage dielectric layer
US6862480B2 (en) 2001-11-29 2005-03-01 Biocontrol Medical Ltd. Pelvic disorder treatment device
US7613516B2 (en) 2001-11-29 2009-11-03 Ams Research Corporation Pelvic disorder treatment device
US20090036946A1 (en) * 2001-11-29 2009-02-05 American Medical Systems, Inc. Pelvic disorder treatments
US20050216069A1 (en) * 2001-11-29 2005-09-29 Biocontrol Medical Ltd. Pelvic disorder treatment device
US6712772B2 (en) 2001-11-29 2004-03-30 Biocontrol Medical Ltd. Low power consumption implantable pressure sensor
US20050049648A1 (en) * 2001-11-29 2005-03-03 Biocontrol Medical Ltd. Pelvic disorder treatment device
US8956295B2 (en) 2002-12-04 2015-02-17 Cardiac Pacemakers, Inc. Sleep detection using an adjustable threshold
US20070161873A1 (en) * 2002-12-04 2007-07-12 Cardiac Pacemakers, Inc. Sleep detection using an adjustable threshold
US8535222B2 (en) 2002-12-04 2013-09-17 Cardiac Pacemakers, Inc. Sleep detection using an adjustable threshold
US20060111626A1 (en) * 2003-03-27 2006-05-25 Cvrx, Inc. Electrode structures having anti-inflammatory properties and methods of use
US7177703B2 (en) * 2003-05-11 2007-02-13 Boveja Birinder R Method and system for providing pulsed electrical stimulation to sacral plexus of a patient to provide therapy for urinary incontinence and urological disorders
US20050143783A1 (en) * 2003-05-11 2005-06-30 Boveja Birinder R. Method and system for providing pulsed electrical stimulation to sacral plexus of a patient to provide therapy for urinary incontinence and urological disorders
WO2005032332A3 (en) * 2003-09-12 2005-08-11 Univ Case Western Reserve Systems and methods for stimulating the pudendal nerve for achieving selective responses.
WO2005032332A2 (en) * 2003-09-12 2005-04-14 Case Western Reserve University Systems and methods for stimulating the pudendal nerve for achieving selective responses.
US7571000B2 (en) 2003-09-12 2009-08-04 Case Western Reserve University Apparatus for stimulating components in, on, or near the pudendal nerve or its branches to achieve selective physiologic responses
US20090326603A1 (en) * 2003-09-12 2009-12-31 Case Western Reserve University Apparatus for stimulating components in, on, or near the pudendal nerve or its branches to achieve selective physiologic responses
US8396555B2 (en) 2003-09-12 2013-03-12 Case Western Reserve University Apparatus for stimulating components in, on, or near the pudendal nerve or its branches to achieve selective physiologic responses
US20060184208A1 (en) * 2003-09-12 2006-08-17 Case Western Reserve University Apparatus for stimulating components in, on, or near the pudendal nerve or its branches to achieve selective physiologic responses
US8606356B2 (en) 2003-09-18 2013-12-10 Cardiac Pacemakers, Inc. Autonomic arousal detection system and method
US9014819B2 (en) 2003-09-18 2015-04-21 Cardiac Pacemakers, Inc. Autonomic arousal detection system and method
US7565198B2 (en) 2004-02-12 2009-07-21 Medtronic Urinary Solutions, Inc. Systems and methods for bilateral stimulation of left and right branches of the dorsal genital nerves to treat dysfunctions, such as urinary incontinence
US8467875B2 (en) 2004-02-12 2013-06-18 Medtronic, Inc. Stimulation of dorsal genital nerves to treat urologic dysfunctions
US20060004421A1 (en) * 2004-02-12 2006-01-05 Bennett Maria E Systems and methods for bilateral stimulation of left and right branches of the dorsal genital nerves to treat dysfunctions, such as urinary incontinence
US8649870B2 (en) 2004-02-12 2014-02-11 Medtronic Uninary Solutions, Inc. Systems and methods including lead and electrode structures sized and configured for implantation in adipose tissue
US7343202B2 (en) 2004-02-12 2008-03-11 Ndi Medical, Llc. Method for affecting urinary function with electrode implantation in adipose tissue
US20080161874A1 (en) * 2004-02-12 2008-07-03 Ndi Medical, Inc. Systems and methods for a trial stage and/or long-term treatment of disorders of the body using neurostimulation
US20050288729A1 (en) * 2004-06-08 2005-12-29 Imad Libbus Coordinated therapy for disordered breathing including baroreflex modulation
US7596413B2 (en) 2004-06-08 2009-09-29 Cardiac Pacemakers, Inc. Coordinated therapy for disordered breathing including baroreflex modulation
US8442638B2 (en) 2004-06-08 2013-05-14 Cardiac Pacemakers, Inc. Adaptive baroreflex stimulation therapy for disordered breathing
US7747323B2 (en) 2004-06-08 2010-06-29 Cardiac Pacemakers, Inc. Adaptive baroreflex stimulation therapy for disordered breathing
US9872987B2 (en) 2004-06-08 2018-01-23 Cardiac Pacemakers, Inc. Method and system for treating congestive heart failure
US20070066995A1 (en) * 2004-06-10 2007-03-22 Ndi Medical, Llc Implantable pulse generator systems and methods for providing functional and/or therapeutic stimulation of muscles and/or nerves and/or central nervous system tissue
US10434320B2 (en) 2004-06-10 2019-10-08 Medtronic Urinary Solutions, Inc. Implantable pulse generator systems and methods for providing functional and/or therapeutic stimulation of muscles and/or nerves and/or central nervous system tissue
US7761167B2 (en) 2004-06-10 2010-07-20 Medtronic Urinary Solutions, Inc. Systems and methods for clinician control of stimulation systems
US10293168B2 (en) 2004-06-10 2019-05-21 Medtronic Urinary Solutions, Inc. Systems and methods for clinician control of stimulation systems
US20100274324A1 (en) * 2004-06-10 2010-10-28 Medtronic Urinary Solutions, Inc. Systems and methods for clinician control of stimulation system
US20070060968A1 (en) * 2004-06-10 2007-03-15 Ndi Medical, Llc Implantable pulse generator systems and methods for providing functional and/or therapeutic stimulation of muscles and/or nerves and/or central nervous system tissue
US7813809B2 (en) 2004-06-10 2010-10-12 Medtronic, Inc. Implantable pulse generator for providing functional and/or therapeutic stimulation of muscles and/or nerves and/or central nervous system tissue
US20050278000A1 (en) * 2004-06-10 2005-12-15 Strother Robert B Implantable pulse generator for providing functional and/or therapeutic stimulation of muscles and/or nerves and/or central nervous system tissue
US8706252B2 (en) 2004-06-10 2014-04-22 Medtronic, Inc. Systems and methods for clinician control of stimulation system
US9724526B2 (en) 2004-06-10 2017-08-08 Medtronic Urinary Solutions, Inc. Implantable pulse generator systems and methods for operating the same
US9308382B2 (en) 2004-06-10 2016-04-12 Medtronic Urinary Solutions, Inc. Implantable pulse generator systems and methods for providing functional and/or therapeutic stimulation of muscles and/or nerves and/or central nervous system tissue
US20070060980A1 (en) * 2004-06-10 2007-03-15 Ndi Medical, Llc Implantable pulse generator systems and methods for providing functional and/or therapeutic stimulation of muscles and/or nerves and/or central nervous system tissue
US9216294B2 (en) 2004-06-10 2015-12-22 Medtronic Urinary Solutions, Inc. Systems and methods for clinician control of stimulation systems
US20070293910A1 (en) * 2004-06-10 2007-12-20 Ndi Medical, Inc. Implantable pulse generator for providing functional and/or therapeutic stimulation of muscles and/or nerves and/or central nervous system tissue
US8195304B2 (en) 2004-06-10 2012-06-05 Medtronic Urinary Solutions, Inc. Implantable systems and methods for acquisition and processing of electrical signals
US9205255B2 (en) 2004-06-10 2015-12-08 Medtronic Urinary Solutions, Inc. Implantable pulse generator systems and methods for providing functional and/or therapeutic stimulation of muscles and/or nerves and/or central nervous system tissue
US8165692B2 (en) 2004-06-10 2012-04-24 Medtronic Urinary Solutions, Inc. Implantable pulse generator power management
US8010209B2 (en) 2005-10-14 2011-08-30 Nanostim, Inc. Delivery system for implantable biostimulator
US20110071586A1 (en) * 2005-10-14 2011-03-24 Nanostim, Inc. Leadless Cardiac Pacemaker Triggered by Conductive Communication
US20070088396A1 (en) * 2005-10-14 2007-04-19 Jacobson Peter M Leadless cardiac pacemaker
US8855789B2 (en) 2005-10-14 2014-10-07 Pacesetter, Inc. Implantable biostimulator delivery system
US8295939B2 (en) 2005-10-14 2012-10-23 Nanostim, Inc. Programmer for biostimulator system
US20110218587A1 (en) * 2005-10-14 2011-09-08 Nanostim, Inc. Programmer for Biostimulator System
US8352025B2 (en) 2005-10-14 2013-01-08 Nanostim, Inc. Leadless cardiac pacemaker triggered by conductive communication
US9072913B2 (en) 2005-10-14 2015-07-07 Pacesetter, Inc. Rate responsive leadless cardiac pacemaker
US20070088418A1 (en) * 2005-10-14 2007-04-19 Jacobson Peter M Delivery system for implantable biostimulator
US7945333B2 (en) 2005-10-14 2011-05-17 Nanostim, Inc. Programmer for biostimulator system
US8457742B2 (en) 2005-10-14 2013-06-04 Nanostim, Inc. Leadless cardiac pacemaker system for usage in combination with an implantable cardioverter-defibrillator
US9168383B2 (en) 2005-10-14 2015-10-27 Pacesetter, Inc. Leadless cardiac pacemaker with conducted communication
US8798745B2 (en) 2005-10-14 2014-08-05 Pacesetter, Inc. Leadless cardiac pacemaker system for usage in combination with an implantable cardioverter-defibrillator
US7937148B2 (en) 2005-10-14 2011-05-03 Nanostim, Inc. Rate responsive leadless cardiac pacemaker
US8788053B2 (en) 2005-10-14 2014-07-22 Pacesetter, Inc. Programmer for biostimulator system
US9687666B2 (en) 2005-10-14 2017-06-27 Pacesetter, Inc. Leadless cardiac pacemaker system for usage in combination with an implantable cardioverter-defibrillator
US9409033B2 (en) 2005-10-14 2016-08-09 Pacesetter, Inc. Leadless cardiac pacemaker system for usage in combination with an implantable cardioverter-defibrillator
US20070088405A1 (en) * 2005-10-14 2007-04-19 Jacobson Peter M Programmer for biostimulator system
US9358400B2 (en) 2005-10-14 2016-06-07 Pacesetter, Inc. Leadless cardiac pacemaker
US8788035B2 (en) 2005-10-14 2014-07-22 Pacesetter, Inc. Leadless cardiac pacemaker triggered by conductive communication
US9192774B2 (en) 2005-10-14 2015-11-24 Pacesetter, Inc. Cardiac pacemaker system for usage in combination with an implantable cardioverter-defibrillator
US20070088397A1 (en) * 2005-10-14 2007-04-19 Jacobson Peter M Leadless cardiac pacemaker system with conductive communication
US9872999B2 (en) 2005-10-14 2018-01-23 Pacesetter, Inc. Leadless cardiac pacemaker system for usage in combination with an implantable cardioverter-defibrillator
US9227077B2 (en) 2005-10-14 2016-01-05 Pacesetter, Inc. Leadless cardiac pacemaker triggered by conductive communication
US10238883B2 (en) 2005-10-14 2019-03-26 Pacesetter Inc. Leadless cardiac pacemaker system for usage in combination with an implantable cardioverter-defibrillator
US20070088400A1 (en) * 2005-10-14 2007-04-19 Jacobson Peter M Rate responsive leadless cardiac pacemaker
US9216298B2 (en) 2005-10-14 2015-12-22 Pacesetter, Inc. Leadless cardiac pacemaker system with conductive communication
US20090069738A1 (en) * 2005-12-29 2009-03-12 Cvrx, Inc. Electrode Structures Having Anti-Inflammatory Properties And Methods Of Use
US9949668B2 (en) 2006-01-10 2018-04-24 Cardiac Pacemakers, Inc. Assessing autonomic activity using baroreflex analysis
US8109879B2 (en) 2006-01-10 2012-02-07 Cardiac Pacemakers, Inc. Assessing autonomic activity using baroreflex analysis
US20070161912A1 (en) * 2006-01-10 2007-07-12 Yunlong Zhang Assessing autonomic activity using baroreflex analysis
US20070260288A1 (en) * 2006-03-03 2007-11-08 Yossi Gross Apparatus for treating stress and urge incontinence
US9889298B2 (en) 2006-03-03 2018-02-13 Astora Women's Health, Llc Electrode sling for treating stress and urge incontinence
US20090043356A1 (en) * 2006-03-03 2009-02-12 Ams Research Corporation Electrode Sling for Treating Stress and Urge Incontinence
US8195296B2 (en) 2006-03-03 2012-06-05 Ams Research Corporation Apparatus for treating stress and urge incontinence
US20090157091A1 (en) * 2006-04-04 2009-06-18 Ams Research Corporation Apparatus for Implanting Neural Stimulation Leads
US20070265675A1 (en) * 2006-05-09 2007-11-15 Ams Research Corporation Testing Efficacy of Therapeutic Mechanical or Electrical Nerve or Muscle Stimulation
US9480846B2 (en) 2006-05-17 2016-11-01 Medtronic Urinary Solutions, Inc. Systems and methods for patient control of stimulation systems
US10322287B2 (en) 2006-05-17 2019-06-18 Medtronic Urinary Solutions, Inc. Systems and methods for patient control of stimulation systems
US20100076254A1 (en) * 2006-06-05 2010-03-25 Ams Research Corporation Electrical muscle stimulation to treat fecal incontinence and/or pelvic prolapse
US20080009914A1 (en) * 2006-07-10 2008-01-10 Ams Research Corporation Systems and Methods for Implanting Tissue Stimulation Electrodes in the Pelvic Region
US8160710B2 (en) 2006-07-10 2012-04-17 Ams Research Corporation Systems and methods for implanting tissue stimulation electrodes in the pelvic region
US20090012592A1 (en) * 2006-07-10 2009-01-08 Ams Research Corporation Tissue anchor
US7647113B2 (en) * 2006-12-21 2010-01-12 Ams Research Corporation Electrode implantation in male external urinary sphincter
AU2007254621B2 (en) * 2006-12-21 2011-05-12 Ams Research Corporation Electrode implantation in male external urinary sphincter
US20080161876A1 (en) * 2006-12-21 2008-07-03 Ams Research Corporation Electrode implantation in male external urinary sphincter
US8774942B2 (en) 2007-07-10 2014-07-08 Ams Research Corporation Tissue anchor
US9427573B2 (en) 2007-07-10 2016-08-30 Astora Women's Health, Llc Deployable electrode lead anchor
US20100049289A1 (en) * 2007-07-10 2010-02-25 Ams Research Corporation Tissue anchor
US8594794B2 (en) 2007-07-24 2013-11-26 Cvrx, Inc. Baroreflex activation therapy with incrementally changing intensity
US20090082828A1 (en) * 2007-09-20 2009-03-26 Alan Ostroff Leadless Cardiac Pacemaker with Secondary Fixation Capability
US9393411B2 (en) 2008-04-02 2016-07-19 Case Western Reserve University System and method of bladder and sphincter control
US20100198288A1 (en) * 2009-02-02 2010-08-05 Alan Ostroff Leadless Cardiac Pacemaker with Secondary Fixation Capability
US8527068B2 (en) 2009-02-02 2013-09-03 Nanostim, Inc. Leadless cardiac pacemaker with secondary fixation capability
US9272155B2 (en) 2009-02-02 2016-03-01 Pacesetter, Inc. Leadless cardiac pacemaker with secondary fixation capability
US20100217340A1 (en) * 2009-02-23 2010-08-26 Ams Research Corporation Implantable Medical Device Connector System
US9539433B1 (en) 2009-03-18 2017-01-10 Astora Women's Health, Llc Electrode implantation in a pelvic floor muscular structure
US20110077708A1 (en) * 2009-09-28 2011-03-31 Alan Ostroff MRI Compatible Leadless Cardiac Pacemaker
US8577472B2 (en) 2009-10-20 2013-11-05 Nyxoah SA Systems and methods for determining a sleep disorder based on positioning of the tongue
US8577464B2 (en) 2009-10-20 2013-11-05 Nyxoah SA Apparatus and methods for feedback-based nerve modulation
US9415215B2 (en) 2009-10-20 2016-08-16 Nyxoah SA Methods for treatment of sleep apnea
US9550064B2 (en) 2009-10-20 2017-01-24 Adi Mashiach Apparatus and methods for feedback-based nerve modulation
US8574164B2 (en) 2009-10-20 2013-11-05 Nyxoah SA Apparatus and method for detecting a sleep disordered breathing precursor
US9409013B2 (en) 2009-10-20 2016-08-09 Nyxoah SA Method for controlling energy delivery as a function of degree of coupling
US11273307B2 (en) 2009-10-20 2022-03-15 Nyxoah SA Method and device for treating sleep apnea
US9943686B2 (en) 2009-10-20 2018-04-17 Nyxoah SA Method and device for treating sleep apnea based on tongue movement
US9415216B2 (en) 2009-10-20 2016-08-16 Nyxoah SA Devices for treatment of sleep apnea
US8380312B2 (en) 2009-12-31 2013-02-19 Ams Research Corporation Multi-zone stimulation implant system and method
US20110160793A1 (en) * 2009-12-31 2011-06-30 Ams Research Corporation Multi-Zone Stimulation Implant System and Method
US9060692B2 (en) 2010-10-12 2015-06-23 Pacesetter, Inc. Temperature sensor for a leadless cardiac pacemaker
US8543205B2 (en) 2010-10-12 2013-09-24 Nanostim, Inc. Temperature sensor for a leadless cardiac pacemaker
US9687655B2 (en) 2010-10-12 2017-06-27 Pacesetter, Inc. Temperature sensor for a leadless cardiac pacemaker
US9020611B2 (en) 2010-10-13 2015-04-28 Pacesetter, Inc. Leadless cardiac pacemaker with anti-unscrewing feature
US10201702B2 (en) 2010-11-30 2019-02-12 Medtronic, Inc. Pelvic floor muscle training
US9126032B2 (en) 2010-12-13 2015-09-08 Pacesetter, Inc. Pacemaker retrieval systems and methods
US11786272B2 (en) 2010-12-13 2023-10-17 Pacesetter, Inc. Pacemaker retrieval systems and methods
US11759234B2 (en) 2010-12-13 2023-09-19 Pacesetter, Inc. Pacemaker retrieval systems and methods
US11890032B2 (en) 2010-12-13 2024-02-06 Pacesetter, Inc. Pacemaker retrieval systems and methods
US8615310B2 (en) 2010-12-13 2013-12-24 Pacesetter, Inc. Delivery catheter systems and methods
US10188425B2 (en) 2010-12-13 2019-01-29 Pacesetter, Inc. Pacemaker retrieval systems and methods
US9242102B2 (en) 2010-12-20 2016-01-26 Pacesetter, Inc. Leadless pacemaker with radial fixation mechanism
US9220887B2 (en) 2011-06-09 2015-12-29 Astora Women's Health LLC Electrode lead including a deployable tissue anchor
US9731112B2 (en) 2011-09-08 2017-08-15 Paul J. Gindele Implantable electrode assembly
US9302093B2 (en) 2011-09-30 2016-04-05 Nyxoah SA Devices and methods for delivering energy as a function of condition severity
US8577466B2 (en) 2011-09-30 2013-11-05 Nyxoah SA System and method for nerve modulation using noncontacting electrodes
US8577467B2 (en) 2011-09-30 2013-11-05 Nyxoah SA Apparatus and method for controlling energy delivery as a function of degree of coupling
US9649493B2 (en) 2011-09-30 2017-05-16 Adi Mashiach System and method for nerve modulation using noncontacting electrodes
US9421372B2 (en) 2011-09-30 2016-08-23 Adi Mashiach Head pain management device having an antenna
US9403009B2 (en) 2011-09-30 2016-08-02 Nyxoah SA Apparatus and methods for implant coupling indication
US9358392B2 (en) 2011-09-30 2016-06-07 Adi Mashiach Electrode configuration for implantable modulator
US9314613B2 (en) 2011-09-30 2016-04-19 Adi Mashiach Apparatus and methods for modulating nerves using parallel electric fields
US8577478B2 (en) 2011-09-30 2013-11-05 Nyxoah SA Antenna providing variable communication with an implant
US8577465B2 (en) 2011-09-30 2013-11-05 Nyxoah SA Modulator apparatus configured for implantation
US9248291B2 (en) 2011-09-30 2016-02-02 Adi Mashiach Hypertension therapy implant apparatus
US9061151B2 (en) 2011-09-30 2015-06-23 Adi Mashiach Apparatus and method to control an implant
US9878159B2 (en) 2011-09-30 2018-01-30 Adi Mashiach Hypertension therapy implant apparatus
US9044612B2 (en) 2011-09-30 2015-06-02 Adi Mashiach Apparatus and method for extending implant life using a dual power scheme
US9895540B2 (en) 2011-09-30 2018-02-20 Nyxoah SA Devices and methods for low current neural modulation
US8989868B2 (en) 2011-09-30 2015-03-24 Hyllio SA Apparatus and method for controlling energy delivery as a function of degree of coupling
US8929999B2 (en) 2011-09-30 2015-01-06 Adi Maschiach Electrode configuration for implantable modulator
US8577468B2 (en) 2011-09-30 2013-11-05 Nyxoah SA Apparatus and method for extending implant life using a dual power scheme
US10828492B2 (en) 2011-09-30 2020-11-10 Adi Mashiach Devices and methods for low current neural modulation
US8588941B2 (en) 2011-09-30 2013-11-19 Nyxoah SA Device and method for modulating nerves using parallel electric fields
US8798773B2 (en) 2011-09-30 2014-08-05 Man & Science, SA Electrode configuration for implantable modulator
US8718776B2 (en) 2011-09-30 2014-05-06 Nyxoah SA Apparatus and method to control an implant
US8700183B2 (en) 2011-09-30 2014-04-15 Nyxoah SA Devices and methods for low current neural modulation
US8644957B2 (en) 2011-09-30 2014-02-04 Nyxoah SA Electrode configuration for implantable modulator
US9511236B2 (en) 2011-11-04 2016-12-06 Pacesetter, Inc. Leadless cardiac pacemaker with integral battery and redundant welds
US11759646B2 (en) 2012-08-01 2023-09-19 Pacesetter, Inc. Biostimulator circuit with flying cell
US10744332B2 (en) 2012-08-01 2020-08-18 Pacesetter, Inc. Biostimulator circuit with flying cell
US9802054B2 (en) 2012-08-01 2017-10-31 Pacesetter, Inc. Biostimulator circuit with flying cell
US11938330B2 (en) 2012-08-01 2024-03-26 Pacesetter, Inc. Implantable leadless pacemakers
US10850090B2 (en) 2013-01-21 2020-12-01 Cala Health, Inc. Devices and methods for controlling tremor
US9452287B2 (en) 2013-01-21 2016-09-27 Cala Health, Inc. Devices and methods for controlling tremor
US10625074B2 (en) 2013-01-21 2020-04-21 Cala Health, Inc. Devices and methods for controlling tremor
US10549093B2 (en) 2014-06-02 2020-02-04 Cala Health, Inc. Method for peripheral nerve stimulation
US10173060B2 (en) 2014-06-02 2019-01-08 Cala Health, Inc. Methods for peripheral nerve stimulation
US10179238B2 (en) 2014-06-02 2019-01-15 Cala Health, Inc. Systems for peripheral nerve stimulation
US10905879B2 (en) 2014-06-02 2021-02-02 Cala Health, Inc. Methods for peripheral nerve stimulation
US10960207B2 (en) 2014-06-02 2021-03-30 Cala Health, Inc. Systems for peripheral nerve stimulation
US10561839B2 (en) 2014-06-02 2020-02-18 Cala Health, Inc. Systems for peripheral nerve stimulation
US9802041B2 (en) 2014-06-02 2017-10-31 Cala Health, Inc. Systems for peripheral nerve stimulation to treat tremor
US12109413B2 (en) 2014-06-02 2024-10-08 Cala Health, Inc. Systems and methods for peripheral nerve stimulation to treat tremor
US10765856B2 (en) 2015-06-10 2020-09-08 Cala Health, Inc. Systems and methods for peripheral nerve stimulation to treat tremor with detachable therapy and monitoring units
US11596785B2 (en) 2015-09-23 2023-03-07 Cala Health, Inc. Systems and methods for peripheral nerve stimulation in the finger or hand to treat hand tremors
US11344722B2 (en) 2016-01-21 2022-05-31 Cala Health, Inc. Systems, methods and devices for peripheral neuromodulation for treating diseases related to overactive bladder
US11918806B2 (en) 2016-01-21 2024-03-05 Cala Health, Inc. Systems, methods and devices for peripheral neuromodulation of the leg
US10814130B2 (en) 2016-07-08 2020-10-27 Cala Health, Inc. Dry electrodes for transcutaneous nerve stimulation
US10610685B2 (en) * 2016-12-21 2020-04-07 University Of Southern California Smooth muscle electrical stimulation based on entrainment of intracellular calcium ion oscillations
US20180169409A1 (en) * 2016-12-21 2018-06-21 University Of Southern California Smooth muscle electrical stimulation based on entrainment of intracellular calcium ion oscillations
US11331480B2 (en) 2017-04-03 2022-05-17 Cala Health, Inc. Systems, methods and devices for peripheral neuromodulation for treating diseases related to overactive bladder
US11857778B2 (en) 2018-01-17 2024-01-02 Cala Health, Inc. Systems and methods for treating inflammatory bowel disease through peripheral nerve stimulation
US11890468B1 (en) 2019-10-03 2024-02-06 Cala Health, Inc. Neurostimulation systems with event pattern detection and classification

Also Published As

Publication number Publication date
GB1434524A (en) 1976-05-05

Similar Documents

Publication Publication Date Title
US3870051A (en) Urinary control
US6937904B2 (en) System and method for providing recovery from muscle denervation
US3667477A (en) Implantable vesical stimulator
US6990376B2 (en) Methods and systems for selective control of bladder function
US6731979B2 (en) Pulse width cardiac pacing apparatus
US6659936B1 (en) Method and apparatus for treating incontinence
US5464429A (en) Apparatus for producing heart defibrillation sequences from stimulation pulses and defibrillation shocks
US6449512B1 (en) Apparatus and method for treatment of urological disorders using programmerless implantable pulse generator system
Tanagho et al. Electrical stimulation in the clinical management of the neurogenic bladder
EP0977615B1 (en) Apparatus for administering microcurrent electrotherapy
CA2336190A1 (en) Implantable stimulator system and method for treatment of urinary incontinence
JPS635763A (en) Heart stimulating apparatus
WO1991019535A1 (en) Method and apparatus for transcutaneous cardiac pacing
CA2120818A1 (en) Regenerative Electrical Stimulator
AU5669200A (en) Electrical stimulation system and methods for treating phantom limb pain and forproviding sensory feedback to an amputee from a prosthetic limb
DE3067650D1 (en) Polyvalent implantable cardiac pacemaker
Sawan et al. Computerized transcutaneous control of a multichannel implantable urinary prosthesis
Haas et al. Neural Stimulation Circuits
Perkins Versatile three-channel stimulation controller for restoration of bladder function in paraplegia
Benvenuto et al. Emergency management of pacemaker failure by means of radio-frequency energy
KR20230126977A (en) Micro current stimulation apparatus for regenerating corneal tissue
Lachance Computerized Transcutaneous Control of a Multichannel Implantable Urinary Prosthesis
AU6141400A (en) Method and apparatus for treating incontinence