Comparison of two different surgical treatment techniques in the treatment of stable vitiligo.
Not Applicable
- Conditions
- Health Condition 1: L80- Vitiligo
- Registration Number
- CTRI/2019/12/022430
- Lead Sponsor
- Armed Forces Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Stable vitiligo patients who give written informed consent
Exclusion Criteria
History of keloid formation, photosensitivity or skin cancer. Pregnant and lactating women, any comorbid diseases, any contraindications to surgical procedures, unstable vitiligo, active infections.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Percentage of repigmentation at specified intervalsTimepoint: six months post procedure
- Secondary Outcome Measures
Name Time Method Repigmentation in vitiligo patchesTimepoint: 2months and 4 months post procedure