EP1872763B1 - Vorrichtung zur prävention und behandlung von störungen des bewegungsapparats - Google Patents

Vorrichtung zur prävention und behandlung von störungen des bewegungsapparats Download PDF

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Publication number
EP1872763B1
EP1872763B1 EP05802488A EP05802488A EP1872763B1 EP 1872763 B1 EP1872763 B1 EP 1872763B1 EP 05802488 A EP05802488 A EP 05802488A EP 05802488 A EP05802488 A EP 05802488A EP 1872763 B1 EP1872763 B1 EP 1872763B1
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EP
European Patent Office
Prior art keywords
pneumatic
pressure
chambers
receiver
foot
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.)
Not-in-force
Application number
EP05802488A
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English (en)
French (fr)
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EP1872763A1 (de
EP1872763A4 (de
Inventor
Anatoly Ivanovich Grigoriev
Inesa Benediktovna Kozlovskaya
Evgeny Petrovich Tihomirov
Elena Illarionovna Sorokina
Evgeniya Nikolaevna Yarmanova
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.)
State Scientific Center Of Russian Fed-Inst Of Bio-Med Probl Of Rus Acad Of Sciences
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State Scientific Center Of Russian Fed-Inst Of Bio-Med Probl Of Rus Acad Of Sciences
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Publication of EP1872763A1 publication Critical patent/EP1872763A1/de
Publication of EP1872763A4 publication Critical patent/EP1872763A4/de
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Publication of EP1872763B1 publication Critical patent/EP1872763B1/de
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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61H—PHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
    • A61H9/00—Pneumatic or hydraulic massage
    • A61H9/005—Pneumatic massage
    • A61H9/0078—Pneumatic massage with intermittent or alternately inflated bladders or cuffs
    • A61H9/0085—Inflated by user's body movement, e.g. ambulatory devices
    • A—HUMAN NECESSITIES
    • A43—FOOTWEAR
    • A43B—CHARACTERISTIC FEATURES OF FOOTWEAR; PARTS OF FOOTWEAR
    • A43B17/00—Insoles for insertion, e.g. footbeds or inlays, for attachment to the shoe after the upper has been joined
    • A43B17/02—Insoles for insertion, e.g. footbeds or inlays, for attachment to the shoe after the upper has been joined wedge-like or resilient
    • A43B17/03—Insoles for insertion, e.g. footbeds or inlays, for attachment to the shoe after the upper has been joined wedge-like or resilient filled with a gas, e.g. air
    • A43B17/035—Insoles for insertion, e.g. footbeds or inlays, for attachment to the shoe after the upper has been joined wedge-like or resilient filled with a gas, e.g. air provided with a pump or valve
    • A—HUMAN NECESSITIES
    • A43—FOOTWEAR
    • A43B—CHARACTERISTIC FEATURES OF FOOTWEAR; PARTS OF FOOTWEAR
    • A43B3/00—Footwear characterised by the shape or the use
    • A43B3/34—Footwear characterised by the shape or the use with electrical or electronic arrangements
    • A—HUMAN NECESSITIES
    • A43—FOOTWEAR
    • A43B—CHARACTERISTIC FEATURES OF FOOTWEAR; PARTS OF FOOTWEAR
    • A43B7/00—Footwear with health or hygienic arrangements
    • A43B7/14—Footwear with health or hygienic arrangements with foot-supporting parts
    • A43B7/1405—Footwear with health or hygienic arrangements with foot-supporting parts with pads or holes on one or more locations, or having an anatomical or curved form
    • A43B7/1455—Footwear with health or hygienic arrangements with foot-supporting parts with pads or holes on one or more locations, or having an anatomical or curved form with special properties
    • A43B7/1464—Footwear with health or hygienic arrangements with foot-supporting parts with pads or holes on one or more locations, or having an anatomical or curved form with special properties with adjustable pads to allow custom fit
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61H—PHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
    • A61H9/00—Pneumatic or hydraulic massage
    • A61H9/005—Pneumatic massage
    • A61H9/0078—Pneumatic massage with intermittent or alternately inflated bladders or cuffs
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61H—PHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
    • A61H2201/00—Characteristics of apparatus not provided for in the preceding codes
    • A61H2201/16—Physical interface with patient
    • A61H2201/1602—Physical interface with patient kind of interface, e.g. head rest, knee support or lumbar support
    • A61H2201/165—Wearable interfaces
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61H—PHYSICAL THERAPY APPARATUS, e.g. DEVICES FOR LOCATING OR STIMULATING REFLEX POINTS IN THE BODY; ARTIFICIAL RESPIRATION; MASSAGE; BATHING DEVICES FOR SPECIAL THERAPEUTIC OR HYGIENIC PURPOSES OR SPECIFIC PARTS OF THE BODY
    • A61H2205/00—Devices for specific parts of the body
    • A61H2205/12—Feet

Definitions

  • the invention relates to the art of medical instrument engineering, and can be suitably used in the medical fields that require prevention or treatment of disorders of locomotion (biomechanics of walking and run).
  • disorders of locomotion biologicals of walking and run.
  • Such disorders generally affect the patients who have not used their legs to support themselves for a long time. These can be a bed-ridden patient or spaceman staying in the zero-gravity state. Neurological patients may also be subjected to such condition.
  • the claimed invention is directed to be used for prevention of such alterations.
  • a device for rehabilitation of the locomotor apparatus in the zero-gravity environment see, e.g. RU Patent 2148981 C1, July 14, 2000 ) whose action on human body is caused by excitation of the human sole receptor zones by the pneumatic-mechanical pressure created in the pulse mode.
  • This device has a number of drawbacks.
  • said device For applying a local pressure on the anatomically characteristic foot zones, said device has two pneumatic boots provided with pneumatic modules. Said “pneumatic boots” have a particular size, and the “pneumatic modules” are positioned therein in strictly determined places that correspond to zones of aggregation of Vater-Pacini corpuscles on the foot sole of a patient to whose size this pneumatic boot is made.
  • the device must be manufactured in view of individual anatomic features of each patient's foot (first of all, sizes of foot length and width, and also possible deformities characteristic of some illnesses are taken into account).
  • the squeezing sleeves that serve to "draw" tightly the pneumatic modules to the sole, operate in beat of delivery of pressure into the pneumatic modules that act on the sole mechanoreceptors, i.e. the device exerts the pulsed mechanical action on the foot both from below and above.
  • the foot is squeezed entirely, and as the sleeves provide the contact surface area greater than that provided by pneumatic modules, then the pressure exerted from above is perceived as being stronger than the pressure acting on the sole.
  • Such squeezing result in the non-physiological, undesired mechanical pressure on the limb, which pressure causes a patient's negative emotional reaction.
  • Said prior-art device has three pneumatic modules for each of the pneumatic boots: 1 being in the calcaneal area, and 2 pneumatic modules (the lateral and medial modules) being for the boot tip portion.
  • Each pneumatic module has its own operation-maintenance system (a separate air-delivery line, a valve, representation in a microprocessor).
  • operation-maintenance system a separate air-delivery line, a valve, representation in a microprocessor.
  • vater-Pacini corpuscles is known to appear in the foot metatarsus zone as two spots (the medial and lateral spots), and there is no functional difference between these aggregations of receptors.
  • Such arrangement of Vater-Pacini corpuscles is caused by the foot anatomy: in these locations the pressure exerted from a support is stronger due to the presence of tubers of the foot sole.
  • the device has two receivers and provides two pressure levels - minimal and maximal levels.
  • the purpose of the device consists in simulation of the physical factors acting on the human foot sole, which factors are characteristic of locomotion in environment of normal gravity. But the pressure acting on the zones of location of Vater-Pacini corpuscles in time of walking or running emerges only in the phase of contact with a support, and any other time this pressure is zero. Said pressure in the device must be released so that to be reduced to the atmospheric pressure. For this reason the presence of the minimal-pressure receiver is not justified in terms of physiology.
  • the claimed device is contemplated to eliminate said drawbacks through use of a different design of said pneumatic boot.
  • the technical objective of the invention consists in provision of a device for prevention and treatment of locomotion disorders, which device will be a more efficient, have an higher manufacturability and be more readily used.
  • a greater efficiency is achieved through a physiologically improved action to be exerted on the receptors, which in turn provides better simulation of the walking or running modes.
  • Said physiologically improved action to be applied by the claimed device is obtained by a more correct pressure to be exerted on a foot owing to elimination of any pressure on the foot dorsal side, and also by elimination of said minimal pressure in the device system.
  • Manufacture and use of the claimed device is rendered more simple and more ready for being used by elimination of the necessity to make any special footwear, and by the possibility to use the user's individual footwear, by exclusion of any second receiver and by exclusion of one pneumatic chamber.
  • each of which boots comprises a means for creating pressure to be exerted on the reflexogenic foot zones, which means is implemented as pneumatic modules consisting of a pneumatic chamber and a pressure source being a compressor with an electric motor, both being connected - through a receiver provided with a pressure sensor and control valves - to each one of the pneumatic chambers; each boot is a user's individual footwear; number of the pneumatic modules for each boot is 2; the compressor and receiver are shared by all pneumatic modules; the receiver through a separate air hose is connected to each one of the pneumatic chambers, said chambers further comprising an electropneumatic valve adapted to supply air therethrough out of the receiver into a pneumatic chamber and to release an excess air out of a pneumatic chamber into atmosphere, as well as to provide the pressure in a pneumatic chamber being equal to the atmospheric pressure; the controlling input of each electropneumatic valve and of each one of the pressure sensors being connected, via an interfacing unit, to
  • the pneumatic chambers being implemented such that when pressure is delivered, they increase their volume only along the vector perpendicular to the plane of the foot sole; shape and sizes of a pneumatic chamber of one of the pneumatic modules correspond to those of the foot metatarsus portion that comprises the medial and lateral areas of Vater-Pacini corpuscles; and shape and size of the second pneumatic module's pneumatic chamber correspond to those of the foot calcaneal portion that also comprises Vater-Pacini corpuscles.
  • the device can be further provided with a display to represent the device performance data.
  • each of which boots comprises a means for creating pressure to be exerted on the reflexogenic foot zones, which means is implemented as pneumatic modules consisting of a pneumatic chamber and a pressure source being a compressor with an electric motor, both being connected - through a receiver provided with a pressure sensor and control valves - to each one of the pneumatic chambers; each boot is a user's individual footwear; number of the pneumatic modules for each boot is 2; the compressor and receiver are shared by all pneumatic modules; the receiver through a separate air hose is connected to each one of the pneumatic chambers, said chambers further comprising an electropneumatic valve adapted to supply air therethrough out of the receiver into a pneumatic chamber and to release an excess air out of a pneumatic chamber into atmosphere, as well as to provide the pressure in a pneumatic chamber being equal to the atmospheric pressure; the controlling input of each electropneumatic valve and of each one of the
  • the pneumatic chambers being implemented such that when pressure is delivered, they increase their volume only along the vector perpendicular to the plane of the foot sole; shape and sizes of a pneumatic chamber of one of the pneumatic modules correspond to those of the foot metatarsus portion that comprises the medial and lateral areas of Vater-Pacini corpuscles; and shape and size of the second pneumatic module's pneumatic chamber correspond to those of the foot calcaneal portion that also comprises Vater-Pacini corpuscles; the pneumatic chambers being implemented in the form of corrugated bellows provided, from below and above, with solid plates; on the upper plate, for the purpose of immediate contact with skin of a user, rigid members are removably positioned; the ratio of surface area of the rigid member and surface area of the front (metatarsal) pneumatic chamber is 1:9, and the ratio of the rigid member's surface area and surface area of the rear (calcaneal) pneumatic chamber is 1:10.
  • the device can be further provided with a display to represent the device performance data.
  • the claimed device is explained in Figs. 1 , 2 , 3 , 4 having the following reference numerals: /1/ - boot, /2/ - electronic-pneumatic unit, /3/ - pneumatic chambers, /4/ - compressor having an electric motor, /5/ - air-supply line, /6/ - receiver, /7/ - receiver's pressure sensor, /8/ - connection hoses, /9/ - an electropneumatic valve of a pneumatic chamber, /10/ - insole, /11/- circuit for controlling an electropneumatic valve, /12/ - pneumatic chambers in the form of corrugated bellows, /13/ - solid plates, /14/ - rigid members, /15/ - microprocessor, /16/ - control valves, /17/ - display.
  • Pneumatic chambers are the sealed chambers made of a rubber cloth, their volume is small, they have a pneumatic connection for connection with conduits extending from the receiver via the pneumatic valves.
  • the lower portion of the pneumatic chambers has an adhesive-pile band glued thereon, using which band said chambers are secured to elastic flexible insole, with the secured complementary portion of said band.
  • the pneumatic chambers on soft insoles are to be inserted into an individual footwear.
  • These insoles are not limited by any structural members, they provide a broader contact with skin as compared with the prototype version; and the pressure distribution from the chamber centre to periphery thereof provides a better simulation of the real pattern.
  • the front chamber is elongated, and its surface area spreads to the medial and lateral zones of Vater-Pacini corpuscle arrangement zones.
  • Insoles are inserted into patient's individual footwear.
  • the compressor of this system must meet rather high requirements. To simulate the action to be exerted in the run pace, the system must create pressure in the pneumatic chamber and release said pressure to zero value in very brief time. Rate of cycles may be frequent, requiring large consumption of air. Any additional volume is adverse under these conditions.
  • simulation of the pressure to be exerted on foot during locomotion represents the natural conditions better.
  • the device has only one receiver configured to maintain a maximal predetermined pressure. Pressure in the pneumatic chambers is released to 0 value.
  • the compressor operates in the stationary mode.
  • the microprocessor is not coupled to the compressor.
  • the pneumatic chambers are connected to the electronic-pneumatic unit (viz. the receiver) through separate tubes.
  • the valves further are electrically connected to the unit, and during the treatment seance, the valves are positioned on the patient's leg in the vicinity of the pneumatic chambers in the sleeve attached to the patient's ankle.
  • the electronic-pneumatic unit causes the device to operate, and controls and monitors the action to be exerted on the foot support zones.
  • the control unit of the device includes the integrally implemented keyboard of 16 film-type keys, and a liquid-crystal display.
  • the control system provides operation of the device in the automatic mode according to a strict cyclogram.
  • the automatic operation mode according to a flexible program allows select different versions of operation of the valves and their interrelated turning-on according to the walking or run cyclogram.
  • the manual mode provides the separate or simultaneous activation of the valves.
  • Pressure in the pneumatic chambers is predetermined as selected by an operator within the range of 0 - 0.5 kgf/cm, increments being 0.001 kg/cm.
  • Liquid-crystal display 20 has two lines that accommodate twenty alphanumeric symbols on each line.
  • the display is adapted to provide imaging of the following information: tuning-on of each one of the valves, a predetermined and current pressure in the receiver, an exerted action mode ("walking-1", “walking-2", “ standing"), a predetermined time period of a cycle, an exerted action, remaining cycle time period.
  • pace of walking (run), duration of single stride, duration of dual stride, duration of the support phase of each leg, duration of the dual-support phase (for walking), duration of the transfer phase, duration of the leap phase (for run); speed of motion being simulated within the following values: for "walking-1" the rate is 75 strides/min, for "walking-2" the rate is 120 strides/min, the run motion rate is 150 strides/min.
  • the operation time period of the claimed system is preset within the range of 1 - 60 min, increments being 1 min long, the cycle time count beginning from the moment a predetermined pressure has been generated in the receiver.
  • Information on turning-on of the valves is duplicated by the light signals emitted by LEDs.
  • the pneumatic chambers can be embodied in 2 versions of their design (the versions may be used depending on goals and capabilities of a user).
  • the calcaneal zone disposed is the chamber whose surface area is 40 - 50 cm 2 , surface area of its contact being 4 - 5 cm 2 , so that ratio of 1:10 is achieved.
  • the contact elements are secured to said plate by means of an adhesive-pile band.
  • the device is complete with a kit of contact elements having various surface area and thickness. Using different thickness of the contact elements, the depth of impression done into the foot soft tissues can be regulated.
  • the device operates as follows.
  • insoles /10/ (the right and left ones) sized to match a patient's individual footwear (boot) /1/.
  • Pneumatic chambers /3/ are secured, using adhesive-pile band, on the pneumatic chambers /10/ on the locations corresponding to disposition of Vater-Pacini corpuscles in the calcaneal and metatarsal zones; and the connecting hoses /8/ extending from the chambers /3/ are brought out of the footwear.
  • the boots /1/ are fastened, tied.
  • the sleeves comprising 2 pneumatic valves /9/ for each leg are positioned on the patient's ankles.
  • the connecting hoses of the pneumatic chambers /8/ are connected to valves /9/.
  • the control circuits from the valves /11/ are coupled separately for the right and left legs through electrical connectors to the microprocessor /15/.
  • the microprocessor /15/ is connected to power supply.
  • a program for exerting action in a givenday is selected by means of the keyboard on the display /17/: a value of the pressure to be created in the chambers; a cycle mode - "walking-1" (75 strides/min), “walking-2” (120 strides/min), run (150 strides/min); a cycle time period. "Start” button is pressed, the program is launched, the compressor (4) starts to operate.
  • a pressure predetermined on the display i.e. on the control unit
  • the control valves (16) open when the pressure sensor (7) sends a signal whose value exceeds a predetermined pressure value.
  • the receiver's pressure sensor communicates with the control valves via the microprocessor (15).
  • the pressure developed in the receiver is delivered, via the outlet tubes (5), into the pneumatic chambers (3) at the moments when the electric valves (11) disposed in the sleeve on the patient's leg are open at their inlet. Pressure out of the chamber is released when a valve is open at its outlet.
  • Electrical communication of the electric valves with control unit (the microprocessor) controller ensures execution of a given program of a seance: rate of activations of each one of 4 pneumatic valves (opening/closure of inlet and outlet), provision of the required time intervals, pauses between activations of 2 valves on each leg, between activations of the valves on the right and left legs - characteristic of the predetermined modes (walking-1, walking-2, run).
  • the device elements are removed off a patient, and the zones wherein said action has been exerted are examined.

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  • Microelectronics & Electronic Packaging (AREA)
  • Footwear And Its Accessory, Manufacturing Method And Apparatuses (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Vehicle Body Suspensions (AREA)
  • Electrical Discharge Machining, Electrochemical Machining, And Combined Machining (AREA)
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  • Orthopedics, Nursing, And Contraception (AREA)

Claims (4)

  1. Vorrichtung zur Prävention und Therapie von Bewegungsstörungen mit zwei Stiefeln (1), wobei jeder Stiefel ein Mittel zum Erzeugen von Druck aufweist, der auf die reflexogenen Fußzonen auszuüben ist, wobei das Mittel als pneumatische Module ausgeführt ist, bestehend aus einer pneumatischen Kammer (3) und einer Druckquelle, die ein Kompressor (4) mit einem Elektromotor ist, die beide über einen mit einem Drucksensor (7) und Steuerventilen (16) versehenen Speicher bzw. Behälter (6) mit jeder der pneumatischen Kammern (3) verbunden sind; dadurch gekennzeichnet, daß jeder Stiefel (1) individuelles Schuhwerk eines Benutzers ist; die Anzahl der pneumatischen Module für jeden Stiefel 2 beträgt;
    der Kompressor (4) und Speicher bzw. Behälter (6) von allen pneumatischen Modulen gemeinsam benutzt werden; der Speicher (6) über einen gesonderten Luftschlauch (5) mit jeder der pneumatischen Kammern (3) verbunden ist, wobei die Kammern ferner ein elektropneumatisches Ventil (9) aufweisen, das geeignet ist, Luft aus dem Speicher bzw. Behälter (6) in eine pneumatische Kammer (3) zu führen und einen Luftüberschuß aus einer pneumatischen Kammer (3) in die Atmosphäre abzugeben sowie den Druck in einer pneumatischen Kammer (3) bereitzustellen, der gleich dem atmosphärischen Druck ist;
    wobei ein Steuereingang jedes elektropneumatischen Ventils (9, 16) und jedes der Drucksensoren (7) über eine Schnittstelleneinheit mit einem Mikroprozessor (15) verbunden ist, der durch ein Programm betrieben wird, das bewirkt, daß die Luft so zugeführt wird, daß verschiebene Arten von Gehen oder Laufen simuliert werden;
    wobei jeder Stiefel (1) ferner eine Einlegesohle (10) aufweist, deren Größen mit den individuellen Benutzerschuhwerkgrößen korrespondieren; die Einlegesohle (10) ein Mittel zum entfernbaren Befestigen der pneumatischen Kammern (3) daran aufweist, wobei die pneumatischen Kammern auf geeigneten Bereichen der Einlegesohle entfernbar positioniert werden;
    wobei die pneumatischen Kammern (3) so ausgeführt sind, daß sie bei Druckzufuhr ihr Volumen nur an dem Vektor entlang vergrößern, der senkrecht zur Ebene der Fußsohle ist;
    Form und Größen einer pneumatischen Kammer (3) eines der pneumatischen Module mit denen des metatarsalen Abschnitts des Fußes korrespondieren, der den Medial- und Lateralbereich von Vater-Pacini-Körperchen aufweist; und Form und Größe der pneumatischen Kammer (3) des zweiten pneumatischen Moduls mit denen des kalkanealen Abschnitts des Fußes korrespondieren, der ebenfalls Vater-Pacini-Körperchen aufweist.
  2. Vorrichtung nach Anspruch 1, dadurch gekennzeichnet, daß die Vorrichtung ferner eine Anzeige (17) aufweist, um die Leistungsdaten der Vorrichtung darzustellen.
  3. Vorrichtung nach Anspruch 1, dadurch gekennzeichnet, daß die pneumatischen Kammern in Form von Faltenbälgen ausgeführt sind, die von unten und oben mit festen Platten (13) versehen sind; auf der oberen Platte steife Teile (14) zum unmittelbaren Kontakt mit Haut eines Benutzers entfernbar positioniert sind; das Oberflächenverhältnis des steifen Teils (14) und der Oberfläche der vorderen, d. h. metatarsalen, pneumatischen Kammer 1:9 beträgt und das Verhältnis der Oberfläche des steifen Teils und der Oberfläche der hinteren, d. h. kalkanealen, pneumatischen Kammer 1:10 beträgt.
  4. Vorrichtung nach Anspruch 3, dadurch gekennzeichnet, daß die Vorrichtung ferner eine Anzeige (17) aufweist, um die Leistungsdaten der Vorrichtung darzustellen.
EP05802488A 2005-04-12 2005-04-12 Vorrichtung zur prävention und behandlung von störungen des bewegungsapparats Not-in-force EP1872763B1 (de)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/RU2005/000188 WO2006110058A1 (fr) 2005-04-12 2005-04-12 Dispositif destine a la prevention et au traitement des troubles de locomotion (et variantes)

Publications (3)

Publication Number Publication Date
EP1872763A1 EP1872763A1 (de) 2008-01-02
EP1872763A4 EP1872763A4 (de) 2010-01-27
EP1872763B1 true EP1872763B1 (de) 2010-12-22

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EP05802488A Not-in-force EP1872763B1 (de) 2005-04-12 2005-04-12 Vorrichtung zur prävention und behandlung von störungen des bewegungsapparats

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EP (1) EP1872763B1 (de)
AT (1) ATE492256T1 (de)
DE (1) DE602005025539D1 (de)
WO (1) WO2006110058A1 (de)

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US8377017B2 (en) 2008-01-03 2013-02-19 Kci Licensing, Inc. Low-profile reduced pressure treatment system
EP2977067B1 (de) 2008-03-13 2020-12-09 3M Innovative Properties Company Vorrichtung zur anwendung von reduzierten druck auf eine gewebestelle eines fusses
US8158844B2 (en) 2008-10-08 2012-04-17 Kci Licensing, Inc. Limited-access, reduced-pressure systems and methods
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RU2148981C1 (ru) * 1999-06-08 2000-05-20 Гришкин Николай Васильевич Устройство для реабилитации опорно-двигательного аппарата в условиях невесомости
IL140315A0 (en) * 2000-12-14 2002-02-10 Medical Dynamics Israel 1998 L Foot compression apparatus

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WO2006110058A1 (fr) 2006-10-19
DE602005025539D1 (de) 2011-02-03
EP1872763A1 (de) 2008-01-02
EP1872763A4 (de) 2010-01-27
ATE492256T1 (de) 2011-01-15

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