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Efficacy Study of Selective Tibial Neurotomy in the Treatment of the Spastic Equinovarus Foot Among Adult Hemiplegic Patients (Neurotomy)

Primary Purpose

Spastic Equinovarus Foot, Stroke

Status
Completed
Phase
Phase 3
Locations
Belgium
Study Type
Interventional
Intervention
Selective tibial neurotomy
Botulinum toxin injection
Sponsored by
Cliniques universitaires Saint-Luc- Université Catholique de Louvain
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Spastic Equinovarus Foot focused on measuring Spastic equinovarus foot, Stroke, Tibial neurotomy, Botulinum toxin type A, Selective tibial neurotomy

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Chronic stroke patients (more than 6 months after stroke)
  • SEF due to spasticity of the calf muscles
  • Positive effects of lidocaïne selective motor nerve block
  • No associated tendinosous retraction: ankle dorsiflexion ≥ 0°after block
  • Insufficient benefit of adaptated kinesitherapy
  • Gait ability allowing an instrumented gait analysis

Exclusion Criteria:

  • Pregnant women
  • BTX injection in the lower limb during the 6 months before inclusion
  • BTX injection in another limb during the 6 months before inclusion
  • patients unable to walk without orthosis on a treadmill

Sites / Locations

  • Université Catholique de Louvain - Cliniques universitaires Saint-Luc

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Neurotomy Group

BTX Group

Arm Description

8 patients undergoing a selective tibial neurotomy under general anesthesia

8 patients undergoing a botulinum toxin injection in the calf muscles under EMG-control

Outcomes

Primary Outcome Measures

Impairments:SIAS,Ashworth and Tardieu scales and MRC scale. Spasticity and gait disorders:muscle stiffness measurement (15) and instrumented gait analysis (11). Disability: ABILOCO scale (16). Participation (quality of life)

Secondary Outcome Measures

Full Information

First Posted
November 14, 2008
Last Updated
December 22, 2011
Sponsor
Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Collaborators
Fonds National de la Recherche Scientifique
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1. Study Identification

Unique Protocol Identification Number
NCT00825097
Brief Title
Efficacy Study of Selective Tibial Neurotomy in the Treatment of the Spastic Equinovarus Foot Among Adult Hemiplegic Patients
Acronym
Neurotomy
Official Title
Study of the Efficacy of the Selective Neurotomy in the Treatment of the Spastic Equinovarus Foot Among Adult Hemiplegic Patient Following the ICF Model. A Prospective, Randomized, Controlled Single Blind Study
Study Type
Interventional

2. Study Status

Record Verification Date
December 2011
Overall Recruitment Status
Completed
Study Start Date
October 2008 (undefined)
Primary Completion Date
December 2011 (Actual)
Study Completion Date
December 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Collaborators
Fonds National de la Recherche Scientifique

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Spastic equinovarus foot (SEF) is a major cause of disability in stroke patients. Treatments may include physical therapy, orthosis, botulinum toxin (BTX) injections and selective neurotomy. Several RCT placebo-controlled studies have demonstrated improvement in spasticity, in pain and in active ankle dorsiflexion after BTX injections. Unfortunately, BTX is an expensive treatment and its effects last about three months. Selective neurotomy consists in a partial section of the motor nerve innervating spastic muscles responsible for the SEF, leading to a permanent treatment of the SEF. Until now, neurotomy has only been assessed by observational case-report studies and has never been submitted to a RCT. The aim of our study is to evaluate the benefits of selective tibial neurotomy in case of SEF according to the 3 domains of the ICF, by comparing it with BTX injections, among a prospective, randomized, controlled single blind study: it would allow to promote a permanent and cost-effective treatment in case of SEF.
Detailed Description
INTRODUCTION Stroke is the third cause of death and the leading cause of handicap among industrialized countries (1). Spasticity following stroke is responsible for spastic equinovarus foot (SEF) in 18% of cases (2). Spastic equinovarus foot is due to spasticity (muscle hypertonia) of the calf muscles (soleus, gastrocnemius and tibialis posterior), often complicated by contracture and by the weakness of peroneus longus and peroneus brevis muscles (3). Therefore, stroke patients walk slowly, and often require assistive device as orthosis or canes. This disability limits their social participation and their quality of life. Spastic equinovarus foot treatments include oral medications, physical therapy, orthosis, chemical denervations (botulinum toxin, alcohol or phenol injections), selective neurotomy and orthopedic surgery (4, 5). Intra-muscular botulinum toxin injection induces a chemical denervation reducing spasticity of injected muscles. Functional block of the neuromuscular junction due to botulinum toxin is reversible and lasts about 3 months. Therefore, this expensive treatment must regularly be administered, with a risk of antibodies development. Selective neurotomy is a neurosurgical procedure consisting in partially and selectively cutting motor branches innervating the spastic muscles. For a low cost, it can permanently reduce muscle spasticity. Botulinum toxin injection effectiveness has largely been demonstrated in spastic equinovarus foot treatment by double-blind randomised controlled trials against placebo (6, 7, 8). Selective tibial nerve neurotomy effectiveness has only been suggested in spastic equinovarus foot treatment by uncontrolled and unrandomised case reports (9, 10, 11). International Classification of Functioning, Disability and Health (ICF) of the World Health Organisation (www.who.int / icidh, 2001) is the framework of the Physical and Rehabilitation Medicine (12). This model describes how a disease can influence patient impairments, activity and participation. Spastic equinovarus foot treatments have already been evaluated in the impairments field: spasticity, muscle strength, walking parameters and gait analysis variables. These treatments should also demonstrate their effectiveness on the patient activity (disability) and on his participation (quality of life). OBJECTIVES The aim of the present project is to study the effectiveness of selective tibial nerve neurotomy on the spastic equinovarus foot, by comparing it with botulinum toxin injection. The functional assessment will explore the three ICF domains. METHODS We will recruit 20 chronic stroke patients presenting with spastic equinovarus foot. This spastic equinovarus foot will be due to calf muscles spasticity without contracture. This spasticity will not have been managed effectively by physical therapy. First, a lidocaïne selective diagnostic motor branch block will systematically be carried out to confirm the treatment indication, and to determine the muscles and / or nerves to treat (14). Once the muscles responsible for the spastic equinovarus foot will be identified, they will surgically or chemically be denervated. Than, patients will be randomized in two groups: One group receiving botulinum toxin injections (toxin group). One group undergoing a neurotomy (neurotomy group). Patients will be assessed before treatment, 2 months and 6 months after treatment among the 3 ICF domains. Impairments will be assessed by the Stoke Impairment Assessment Set (SIAS), the Ashworth and Tardieu scales (spasticity) and the MRC scale (muscle strength). Spasticity and gait disorders will quantitatively and objectively be evaluated by the muscle stiffness measurement (15) and an instrumented gait analysis (11). Disability will be evaluated by the ABILOCO scale (16) and the participation (quality of life) by the StrokeQol scale (17) and the SF-36 questionnaire. The patients selection, the lidocaïne hyperselective diagnostic blocks, the botulinum toxin injections and the selective neurotomies will be achieved at Cliniques universitaires Mont-Godinne. The functional assessment (clinical evaluation, gait analysis, muscle stiffness measurement) will be achieved in the Physical Medicine and Rehabilitation department (READ unit) by a blinded assessor. PERSPECTIVE From this study, we hope to demonstrate the effectiveness of the selective neurotomy in spastic equinovarus foot treatment among the 3 ICF domains (impairment, activity and participation). This should promote this effective, permanent and cheap spastic equinovarus foot treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Spastic Equinovarus Foot, Stroke
Keywords
Spastic equinovarus foot, Stroke, Tibial neurotomy, Botulinum toxin type A, Selective tibial neurotomy

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
16 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Neurotomy Group
Arm Type
Experimental
Arm Description
8 patients undergoing a selective tibial neurotomy under general anesthesia
Arm Title
BTX Group
Arm Type
Active Comparator
Arm Description
8 patients undergoing a botulinum toxin injection in the calf muscles under EMG-control
Intervention Type
Procedure
Intervention Name(s)
Selective tibial neurotomy
Intervention Description
Selective tibial neurotomy is a neurosurgical intervention consisting in partially and selectively cutting the motor nerve branches destinated to the spastic muscles.
Intervention Type
Drug
Intervention Name(s)
Botulinum toxin injection
Intervention Description
Botulinum toxin type A
Primary Outcome Measure Information:
Title
Impairments:SIAS,Ashworth and Tardieu scales and MRC scale. Spasticity and gait disorders:muscle stiffness measurement (15) and instrumented gait analysis (11). Disability: ABILOCO scale (16). Participation (quality of life)
Time Frame
Before treatment (T0); 2 months (T1) and six months (T2) after treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Chronic stroke patients (more than 6 months after stroke) SEF due to spasticity of the calf muscles Positive effects of lidocaïne selective motor nerve block No associated tendinosous retraction: ankle dorsiflexion ≥ 0°after block Insufficient benefit of adaptated kinesitherapy Gait ability allowing an instrumented gait analysis Exclusion Criteria: Pregnant women BTX injection in the lower limb during the 6 months before inclusion BTX injection in another limb during the 6 months before inclusion patients unable to walk without orthosis on a treadmill
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Benjamin Bollens, Doctor
Organizational Affiliation
Université Catholique de Louvain
Official's Role
Principal Investigator
Facility Information:
Facility Name
Université Catholique de Louvain - Cliniques universitaires Saint-Luc
City
Brussel
ZIP/Postal Code
1200
Country
Belgium

12. IPD Sharing Statement

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Efficacy Study of Selective Tibial Neurotomy in the Treatment of the Spastic Equinovarus Foot Among Adult Hemiplegic Patients

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