COMPARATIVE STUDY OF THE EFFICACY AND SAFETY OF 10% RETINOL PEEL AND 70% GLYCOLIC ACID PEEL IN THE TREATMENT OF ACANTHOSIS NIGRICANS
Phase 3
- Conditions
- Health Condition 1: L83- Acanthosis nigricans
- Registration Number
- CTRI/2023/09/057674
- Lead Sponsor
- CHERUKUPALLI ANANTH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
CLINICALLY DIAGNOSED AND CONSENTING PATIENTS WITH ACANTHOSIS NIGRICANS
Exclusion Criteria
1. Patients with Post inflammatory hyperpigmentation and other facial dermatoses.
2. Pregnant and Lactating women.
3. Patients who are on topicals/systemic retinoids and other de-pigmenting agents.
4. Non-consenting patients.
5. Patients with unrealistic expectations.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. To determine the efficacy and safety of 10% Retinol peel in the treatment of Acanthosis Nigricans. <br/ ><br>2. To determine the efficacy and safety of 70% Glycolic acid peel in the treatment of Acanthosis Nigricans. <br/ ><br>3. To compare the efficacy and safety of the following two treatment options.Timepoint: 2.5 MONTHS
- Secondary Outcome Measures
Name Time Method 1. Acanthosis Nigricans Area and Severity Index (ANASI) <br/ ><br>2. Investigator’s Global Evaluation (IGE) scale. <br/ ><br>3. Participant’s Global Evaluation (PGE) scale. <br/ ><br>4. Cutaneous adverse reactions scale. <br/ ><br>5.Dermatoscopic findings.Timepoint: 2.5 MONTHS