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Assessment of The Effect of Milk_Aftimoon on Melasma

Phase 3
Conditions
Melasma.
Melasma
Registration Number
IRCT2016030826967N1
Lead Sponsor
Shahid Beheshti University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
70
Inclusion Criteria

Patients with Melasma who would like to participate in the study including men and women aged 18 to 65 years with duration of the disease more than 6 months.
Exclusion criteria: breastfeeding; pregnancy; intolerance to milk; hormonal disorders (Cushing, Hyperthyridism, Addisons Disease); use of anti stain drugs in the past three months; performance of procedures using chemical peels; microderm abrasion done in the last three months; performance of laser thrapy in the last three months; carrying out intense sun tanning or sunburns in three recent months; suffering from hemorroids; pulmonary problems; taking medicine for other disease.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Dermacatch Changes. Timepoint: Before Treatment, One and Three Months After Begining treatment. Method of measurement: Erythma and Melanin Determinding by Dermacatch.
Secondary Outcome Measures
NameTimeMethod
Clinical Disease Progression. Timepoint: Before Treatment One and Three Month After Begining treatment. Method of measurement: Targeted Assessment Practitioner(with Comparisons and Review Photo).;MASI Score. Timepoint: Before Treatment, One and Three Months After Begining of Treatment. Method of measurement: Erythema and Color Measurment by Physician.
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