Comparison of suction blister and micro punch grafting methods in the treatment of patients with stable vitiligo
Not Applicable
- Conditions
- Vitiligo.Vitiligo
- Registration Number
- IRCT20210206050270N1
- Lead Sponsor
- Vice Chancellor for Research, Isfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 31
Inclusion Criteria
Patients with persistent vitiligo are resistant to medical treatment, ie they have not had a new lesion in the past year and their previous lesions have not become larger.
Patients should be between 13 and 65 years old
Patients must give informed consent
Patients should be willing to cooperate during the study and follow-up period.
Exclusion Criteria
Patients with immunodeficiency
atients with bleeding disorders
Patients being treated for other illnesses
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Having Complaints. Timepoint: 2 and 4 months after treatment. Method of measurement: questionnaire- visual analog scale (VAS).;Improvement Score. Timepoint: 2 and 4 months after treatment. Method of measurement: questionnaire-visual analog scale (VAS).;Satisfaction Score. Timepoint: 2 and 4 months after treatment. Method of measurement: questionnaire -visual analog scale (VAS).
- Secondary Outcome Measures
Name Time Method