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Effect of botulinum toxin on Raynaud's phenomenon in patients with systemic sclerosis

Not Applicable
Conditions
Raynaud&#39
s phenomenon
Registration Number
JPRN-UMIN000019985
Lead Sponsor
Gunma University Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
40
Inclusion Criteria

Not provided

Exclusion Criteria

Patients under the age 18, 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
NameTimeMethod
The change in severity of RP, including the frequency, pain, color and duration, by the Raynaud score and VAS at 4 weeks after treatment compared with the baseline.
Secondary Outcome Measures
NameTimeMethod
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