Effect of topical fluorouracil on vitiligo
Phase 2
Recruiting
- Conditions
- vitiligo.Vitiligo
- Registration Number
- IRCT20180602039939N1
- Lead Sponsor
- Mashhad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 25
Inclusion Criteria
Age above 10 years
Refractory lesions after 3 month of NB-UVB therapy
Lesions distal to elbow/knee (except palms and soles)
Signed written informed consent
Exclusion Criteria
Active cobner phenomenon at the lesion site
Active infection at the lesion site
Lesions more than 10 cm
Pregnancy/breastfeeding
Bleeding diseases
Immunosuppress patients
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Re-pigmentation ratio;. Timepoint: Each 2 weeks until 3 months. Method of measurement: Scoring according to the dermatologist diagnosis.
- Secondary Outcome Measures
Name Time Method Re-pigmentation start time. Timepoint: Each 2 weeks until 3 months. Method of measurement: Scoring according to dermatologist diagnosis.