A study to compare the efficacy two chemical peels in post acne pigmentatio
Not Applicable
- Conditions
- Health Condition 1: L00-L99- Diseases of the skin and subcutaneous tissue
- Registration Number
- CTRI/2019/05/019315
- Lead Sponsor
- Dr Bharathi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Closed to Recruitment of Participants
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.All patients with post acne pigmentation
2.Those who give written consent for the study
Exclusion Criteria
1.Pregnant and Lactating women
2.Females using oral contraceptives 3.History of taking Oral Isotretinoin 4.Patients with active herpes simplex infection or active acne lesions(pustules, nodules and cysts) 5.Patients with pre existing skin lesions over the study site
6.Patients with h/o keloidal tendency(ie any previous h/o vaccination/surgery induced scars).
7.Patients with unrealistic expectations.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Reduction in Physical Global Assessment Score at 6 weeks, after completing full course of treatment.Timepoint: 6 weeks
- Secondary Outcome Measures
Name Time Method Reduction in downtime between two groupsTimepoint: 6 weeeks