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Evaluaion of tolerability and efficacy of Melatrance lightening cream for the treatment of melasma

Phase 2
Recruiting
Conditions
Melasma.
Chloasma
L81.1
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
Inclusion Criteria

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

Exclusion Criteria

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
NameTimeMethod
Modified melasma severity index. Timepoint: Before intervention, 6 weeks later and 12 weeks after intervention. Method of measurement: Using mMASI index.
Secondary Outcome Measures
NameTimeMethod
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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