Clinical evaluation of different topical formulations of Fumaria officinalis extract on the Vitiligo and analysis of its Fumaric acid content by HPLC.
Phase 2
- Conditions
- vitiligo.disorders of pigmentation
- Registration Number
- IRCT201111108022N1
- Lead Sponsor
- Vice chancellor for research, Kermanshah University Of Medical Sciences and Health Services
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 75
Inclusion Criteria
lasting more than 6 month after diagnosis, age 11-60, filling informed consent. Exclusion criterion: Pregnancy, Lactation, not filling consent form.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Repigmentation rate after treatment. Timepoint: Every 2weeks during 4 months. Method of measurement: Observtion.
- Secondary Outcome Measures
Name Time Method Diameter reduction. Timepoint: every 2 weeks during 4 months. Method of measurement: Evaluation of diameter with precise measurement.