Evaluaion of tolerability and efficacy of Melatrance lightening cream for the treatment of melasma
- Conditions
- Melasma.ChloasmaL81.1
- Registration Number
- IRCT20190210042676N25
- Lead Sponsor
- Knowledge-based company of Janus
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 20
18 - 50 years old men and women
Cases of mild to moderate melasma (MGSC=1& 2)
General health
Signing the consent form for participation in the study
Documented allergies to components of cream
Use of topical lightening products like AHA ,BHA and retinoid component within 21 days prior to the study
Pregnancy or lactating
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Modified melasma severity index. Timepoint: Before intervention, 6 weeks later and 12 weeks after intervention. Method of measurement: Using mMASI index.
- Secondary Outcome Measures
Name Time Method Skin melanin content changes. Timepoint: Before intervention,6 and 12 weeks after using. Method of measurement: mexameter.;Size and amount of skin spots. Timepoint: Before intervention, 6 and 12 weeks after using. Method of measurement: Visio face.
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