CRYOSTROKE study is designed : * to compare the efficacy and safety of percutaneous CryoNeurotomie (CN) versus surgical neurotomy (SN) on spasticity, 90 days after intervention, in post-stroke patients presenting with spastic equinovarus foot and, * to ensure that potential clinical effect/safety remain stable within time, with a 12-month follow-up.
Stroke, arising from cerebral vascular hemorrhage or ischemia, represents a major health-care problem affecting more than 140,000 persons in France every year. One of the major concerns after stroke is impairment of the pyramidal tract and parapyramidal fibers, resulting in upper motor neuron syndrome and spasticity. Up to 20% to 40% of stroke survivors develop spasticity, which dramatically impacts health status, pain, functional capacity, and ultimately, quality of life. Spastic equinovarus foot (SEF) is the most common deformity due to lower limb spasticity and is defined as a combination of an abnormal plantar-flexion, inversion and adduction of the foot. Consequently, SEF severely impairs walking capability and mobility, impacting daily life activities and restricting social participation. In addition to therapeutical physical rehabilitation programs, two main treatments can be proposed. First, SEF can be initially treated with focal botulinum toxin injections that for reducing spasticity. However, botulinum toxin injections are effective for only a limited period of time, and iterative reinjections are required. Second, permanent treatment of spasticity can be achieved by surgical neurotomy. This procedure, variably combined with muscle and tendon lengthening in the event of associated retractions, can be considered as the long-term radical and effective gold standard, but at the price of surgical invasiveness and complications. A recent alternative allowing for both permanent treatment and a minimally invasive approach has been introduced: "percutaneous cryoneurotomy". While this approach has provided promising results, as shown in multiple case reports, its efficacy has yet to be determined in a randomized control study. CryoNeurotomy (CN) was first performed and developed in daily practice for the upper limb. Through a mentoring process, a feasibility study was performed on cadavers and transposed the technique to human procedures in a pilot study. The results from the first patients, with a 90-day follow-up period, are promising, with decreased spasticity and significantly increased walking capabilities. Major potential advantages of percutaneous CN compared to surgical neurotomy were identified, such as minimal skin incision, faster procedure, far less invasiveness of muscle tissue and adjacent neuro-vascular structures, particularly a decreased risk of post-operative sensory loss or neuropathic pain, no need for general anesthesia (local anesthesia) and possible performance on an outpatient basis. By enlarging Physical Medicine and Rehabilitation (PMR) therapeutical armamentarium, percutaneous CN could represent a new compromise between botulinum toxin iterative injections and radical surgery, in terms of invasiveness \& complications/long-term benefit ratio on spasticity and function. The CRYOSTROKE study was designed: * to compare the efficacy and safety of percutaneous CN versus surgical neurotomy on spasticity, 90 days after intervention, in post-stroke patients presenting with spastic equinovarus foot and, * to ensure that potential clinical effect/safety remain stable within time, with a 12-month follow-up.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
114
Surgical neurotomy will be performed under general anesthesia according to the previous description. Muscle relaxant drugs will not be used in order to prevent any interference with the intraoperative electrical stimulation. The patient will be placed in a prone position and a vertical cutaneous incision will be made at the popliteal fossa location. The tibial nerve will be dissected and the motor nerve branches of the soleus, gastrocnemius, tibialis posterior and flexor hallucis longus will be identified with intraoperative tripolar electrical stimulation. The selected motor nerve branches will be partially sectioned over a 5mm length under the microscope. The extent of nerve section will be determined according to the degree of spasticity and to the intraoperative residual muscular contraction under electrical stimulation
After the use of an aseptic technique with 2% chlorhexidine, betadine application and a local anesthesia with lidocaine 1% (3ml), percutaneous cryoneurotomy will be performed with METRUM CRYOFLEX device guided by ultrasound with 1.2mm cryoprobe at -89°C placed through a #16 angio guide. Electrical stimulation will be performed to confirm tibial nerve contact at 0.8 mV. The ice ball will be repositioned to two spots along the nerve. Each lesion will be treated for 2min cryoneurolysis at -89°C, followed by 2min without freezing (passive defreezing period) and 2min of cryoneurolysis at -89°C, based on cryotherapy for pain management.
Hôpital Raymond Pointcarré
Garches, France
RECRUITINGCHRU Montpellier
Montpellier, France
NOT_YET_RECRUITINGC.H.U. Poitiers
Poitiers, France
NOT_YET_RECRUITINGCHU Rennes
Rennes, France
NOT_YET_RECRUITINGPôle Saint-Hélier
Rennes, France
NOT_YET_RECRUITINGCHU Saint-Etienne
Saint-Etienne, France
NOT_YET_RECRUITINGHôpital Purpan
Toulouse, France
NOT_YET_RECRUITINGMean absolute change in spasticity assessed by the Modified Ashworth Scale (MAS) ranging from 0 (no spasticity) to 4 (maximum spasticity).
Mean absolute change in spasticity assessed by the Modified Ashworth Scale (MAS) ranging from 0 (no spasticity) to 4 (maximum spasticity). This MAS will be quantified on a passive ankle dorsal flexion with knee extended (180°) movement.
Time frame: Between baseline and 90-day follow-up
Mean absolute change in functional disability assessed using the Barthel Index (BI).
Time frame: Between baseline and 90, 180 and 365-day follow-ups
Mean absolute change in passive ankle dorsal flexion with knee flexed (90°) and extended (180°) movement spasticity assessed by the Modified Ashworth Scale (MAS)
Time frame: Between baseline and 90, 180 and 365-day follow-ups
Mean absolute change in muscle's response to stretch applied at given velocities assessed by the Tardieu Scale and the Modified Tardieu Scale (MTS)
Time frame: Between baseline and 90, 180 and 365-day follow-ups
Mean absolute change in maximal ankle range of motion (in degrees) assessed with a goniometer in slow and rapid movement
Time frame: Between baseline and 90, 180 and 365-day follow-ups
Mean absolute change in the Medical Research Council (MRC) scale of muscle strength of the impaired foot.
Time frame: Between baseline and 90, 180 and 365-day follow-ups
Mean absolute change in time in seconds to complete the 10-meter walking test
Time frame: Between baseline and 90, 180 and 365-day follow-ups
Mean absolute change in the distance in meters covered in the 6-min walking test
Time frame: Between baseline and 90, 180 and 365-day follow-ups
Physical activity intensities: Mean absolute change in the rate of high, moderate, light activities bet
Time frame: Between baseline and 90, 180 and 365-day follow-ups for a period of 7 days before each visit
Physical activity intensities: mean absolute change in number of steps measured with accelerometer (ActiGraph GT9X)
Time frame: Physical activity intensities: mean absolute change in number of steps measured with accelerometer (ActiGraph GT9X)
Mean absolute change in pain surface using a digital mapping tool converting pain drawings to cm²
Time frame: Between baseline and 90, 180 and 365-day follow-ups
Mean absolute change in pain intensity and interference using the Brief Pain Inventory (BPI) questionnaire
Time frame: Between baseline and 90, 180 and 365-day follow-ups
Mean absolute change in quality of life: EuroQol 5 Dimensions 5 Levels (EQ-5D-5L) questionnaire
Time frame: Between baseline and 90, 180 and 365-day follow-ups
Mean absolute change in fatigue: Brief Fatigue Inventory (BFI) questionnaire
Time frame: Between baseline and 90, 180 and 365-day follow-ups
Mean goal attainment assessed with the Goal Attainment Scale (GAS) consisting in 3 main goals provided by the patient before intervention
Time frame: Between baseline and 90, 180 and 365-day follow-ups
Mean patient satisfaction assessed with Patient Global Impression of Change Patient satisfaction (PGIC)
Time frame: Between baseline and 90, 180 and 365-day follow-ups
Medico-economic impact measured with Health Care Utilization (HCU) costs
Time frame: From baseline to 365-day post intervention in terms
Medico-economic impact measured with Employment status
Time frame: From baseline to 365-day post intervention in terms
Medico-economic impact measured with medication intake
Time frame: From baseline to 365-day post intervention in terms
Rates of adverse events & serious adverse events
Time frame: From baseline to 365-day post intervention in terms
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