efficacy of skin pigment suspension in treatment of white burn scars
Phase 2
- Conditions
- post-burn leukoderma.Leukoderma, not elsewhere classified
- Registration Number
- IRCT2016013026269N1
- Lead Sponsor
- Vice Chancellor for research of Isfahan University of Medical Sciences.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 42
Inclusion Criteria
Age =18 years; Non-pregnant and non-breast feeding women; without history of chronic diseases, skin cancer, drug sensitivity/sever allergic reactions, immun deficient, organ transplant or steroid treatment; The absence of coagulopathy or anticoagulation therapy; No evidence of hypertrophic burn scar; The total area treated is >40 cm2. Exclusion criteria: Previous treatment of skin lesions; Active systemic infection.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Repigmentation scales. Timepoint: one, three and six months after the end of treatment. Method of measurement: by dermatology Colleagues blinded to the randomization.
- Secondary Outcome Measures
Name Time Method Edema, Erythema, Infection and Dyspigmentation. Timepoint: One week, ane month, three months and six months after treatment. Method of measurement: Eye Clinical Evaluation.