Effect of botulinum toxin on Raynaud's phenomenon in patients with systemic sclerosis
Not Applicable
- Conditions
- Raynaud's phenomenon
- Registration Number
- JPRN-UMIN000024135
- Lead Sponsor
- Gunma University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 2
Inclusion Criteria
Not provided
Exclusion Criteria
Patients under the age 16, with the pregnancy or having the past medical histories with BTX were excluded.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The change in severity of RP, including the frequency, pain, color and duration, by the Raynaud's condition score at 4 weeks after treatment compared with the baseline.
- Secondary Outcome Measures
Name Time Method The change in severity of RP, including the frequency, pain, color and duration, by the Raynaud's condition score at 8, 12, 16 weeks after treatment compared with the baseline.