Microneedling plus topical 5-FU in treatment of Vitiligo
Phase 3
Recruiting
- Conditions
- Vitiligo.Vitiligo
- Registration Number
- IRCT20200506047320N1
- Lead Sponsor
- Ahvaz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
All patients with stable vitiligo
Exclusion Criteria
Pregnancy and lactation
Age under 10 y
Lesions on face, genitalia and intertriginous areas
Active Koebner phenomenon
Coagulopathy
Active infection
Previous history of keloid or high risk for keloid
Drug hypersensitivity
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Repigmentation level in Vitiligo lesions. Timepoint: At beggining of study and then after treatmen starts every 2 weeks for 3 months. Method of measurement: Based on the percentage of repigmentation and classification as 0 to 25 percent, 25 to 50, 50 to 75 and above 75 percent.
- Secondary Outcome Measures
Name Time Method