The study for the effect of botulinum toxin for upper limb spasticity
Not Applicable
Recruiting
- Conditions
- Stroke chronic phase
- Registration Number
- JPRN-jRCT1090220265
- Lead Sponsor
- Toru Takekawa
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Chronic stroke patient with upper limb spasticity after six months after attack.
Exclusion Criteria
Patients With dementia, with cognitive disorder, who cannot do rehabilitation exercise, in whom BOTOX is contraindicated as specified in the package insert of BOTOX.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method