Comparative evaluation of efficacy of multiple treatments in the treatment of vitiligo
Phase 3
- Conditions
- vitiligo.disorder of pigmentation
- Registration Number
- IRCT138904081159N6
- Lead Sponsor
- Vice chancellor for research, Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 70
Inclusion Criteria
Inclusion Criteria:
1- Having no treatment within past 6 months
2- Men or women of 11-60 years old
3- Have a diagnosis of vitiligo with depigmented patch more than 5 cm despite receiving at least 3 months active treatment
4- Stable vitiligo for at least 1 year
5- No infection at recipient site
6- No history of keloid and or koebner phenomenon
7- No history of active hepatitis the B, C, or AIDS
8- No pregnancy or breast-feeding
9- No active uncontrolled chronic systemic disease
Exclusion Criteria
Vitiligo patients with active or progressive disease within last 12 months.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pigmentation. Timepoint: Before intervention and 1 week, 3 weeks, 1 month and 3 months after transplantation. Method of measurement: Observation, wood lamp, visioface software.
- Secondary Outcome Measures
Name Time Method