Comparison the Effect of Three Different Type of Treatment in Patients Being Treated for Vitiligo Lesions: 1. Microneedling, 2. Microneedling with Topical Fluocinolone and 3. Microneedling with 5-F
Not Applicable
Recruiting
- Conditions
- Vitiligo.Vitiligo
- Registration Number
- IRCT20220806055626N1
- 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 without new lesions in the previous six months who have read and signed the consent form
Exclusion Criteria
Pregnant Women
Lactating Mothers
Facial lesions, genitalia and wrinkled areas
Active koebner phenomenon
Having coagulation diseases
Patients with active infection
Patient with high risk of keloid and previous history of keloid
Presence of sensitivity to the study drugs
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Vitiligo lesions repigmentation. Timepoint: At the beginning of the study; After starting the study every week for three months; Three and six months after completing the study. Method of measurement: The amount of change in the area of the lesion after treatment by examining the photos in color analysis software.
- Secondary Outcome Measures
Name Time Method G-score. Timepoint: After the beginning of repigmentation every week, every month after the end of the study for up to six months. Method of measurement: Color analysis software.;Repigmentation start time. Timepoint: After starting to study, every week. Method of measurement: Observing the color change through photo analysis.