Strategy to Adapt Botulinum Toxin Doses in Dystonia
Not yet recruiting
- Conditions
- Dystonia
- Registration Number
- NCT06386848
- Lead Sponsor
- Central Hospital, Nancy, France
- Brief Summary
The study is designed to observ and collect the doses of botulinum toxin injected in dystonia in different centres to compare the initial dose and the dose recommended.
We we ll study the increase of the dose injected over the time, the side effects...
The hypothesis is that we inject smaller doses than we could regarding the recommandations
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
- patients over 18 years old followed for dystonia and treated with botulinum toxin
Exclusion Criteria
- first dose of botulinum toxin not available
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method First dose of botulinum toxin injected, U 30 years dose injected in U
- Secondary Outcome Measures
Name Time Method Effective dose of botulinum toxin 30 years dose injected in U
Side effects 30 years diplopia, ptosis and others