Functional effects of botulinum toxin in the hip adductors and subsequent exercise in HSP patients
- Conditions
- Hereditary Spastic ParaplegiaTherapeutic area: Diseases [C] - Nervous System Diseases [C10]
- Registration Number
- EUCTR2015-003184-11-NL
- Lead Sponsor
- Radboud University Medical Centre
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- Not specified
- Target Recruitment
- 30
-diagnosis of pure HSP based on molecular diagnosis (e.g. SPG-4 mutations) or based on inheritance
-age at least 18 years
-suffer from (bilateral) hip adductor spasticity without contracture (modified Ashworth scale score 1-4)
-being a minimally independent household ambulator without walking aid (Functional Ambulation Categories 4-5)
-gait velocity > 0.4 m/s
-complain of balance problems due to a narrow base of support or problems with lateral stepping
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 30
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range
-Last BTX treatment of the hip adductors is shorter than 6 months ago or when a next BTX treatment of these muscles cannot be postponed for 4 months without increasing fall risk or jeopardizing patients’ safety in any other way.
-Any previous BTX injections in the calf muscles are accepted, but it must be possible to safely postpone subsequent injections of these muscles for 4 months after inclusion
-Insufficient vision
-Insufficient cardiopulmonary endurance
-Insufficient sensorimotor abilities
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Main Objective: The primary objectives of this study is to investigate whether BTX injections, injected bilaterally in the spastic adductors of patients with HSP can improve lateral stepping and gait width. ;Secondary Objective: The secondary objectives are balance confidence, Berg Balance Scale, comfortable and maximum overground gait velocity, 6-Min Walk Test, Timed Up and Go test and gait adaptability.;Primary end point(s): Increased succesratio of recovering balance by a lateral step. Increased frontal leg angle. Increased gait width;Timepoint(s) of evaluation of this end point: before, 6 weeks and 16 weeks after the injection
- Secondary Outcome Measures
Name Time Method Secondary end point(s): Increased balance confidence, gait velocity and gait adaptability;Timepoint(s) of evaluation of this end point: before, 6 weeks and 16 weeks after the injection