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Comparing Glycolic Acid Peel and Cream for treating Melasma

Effectiveness of Fortnightly 35 percent Glycolic Acid Peel Versus Daily 12 percent Glycolic Acid Cream in the Treatment of Melasma: A Prospective, Comparative, Two-arm, Double-blind, Randomised Controlled Study at a Tertiary Care Centre in Mandya

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/10/096111
Enrollment
30
Registered
2025-10-15
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: L811- Chloasma

Interventions

Intervention1: 35 percent Glycolic acid peel: The intervention agent in this study is Glycolic Acid 35 percent (w/v) peel, an Alpha Hydroxy Acid (AHA) chemical peel administered every two weeks under

Sponsors

Dr Shashikumar B M
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients diagnosed with melasma. Patients aged 18-65 years of both sexes. Patients who are not on active treatment and not taken any treatment for melasma in the past 1 month. Patients willing to give informed consent to participate in the study.

Exclusion criteria

Exclusion criteria: Pregnant and lactating females. Hypersensitivity to the peeling agent. Skin infection at the site of Melasma (herpes, pyoderma, and folliculitis). Patients with topical steroid damaged face. Patients with rosacea, systemic lupus erythematosus and other photodermatoses. Patients consuming Oral contraceptive pills. Patients with unrealistic expectations. Patients consuming Isotretinoin tablets and other drug which can cause and exuberate melasma. History of keloids or hypertrophic scars. Concomitant skin or systemic disease.

Design outcomes

Primary

MeasureTime frame
•Change in MASI (Melasma Area and Severity Index) score.Timepoint: •From baseline( Day 0) to 4, 8, and 12 weeks.

Secondary

MeasureTime frame
Grading of subjective improvement in pigmentation, assessed as no response, mild, moderate, good, or very good response based on MASI score reduction.Timepoint: Before treatment and at the completion of the study (end of 12 weeks, after the sixth peel/last follow-up visit)

Countries

India

Contacts

Public ContactDr Deepadarshan K

Mandya institute of medical sciences

deepadarshan.rani@gmail.com9844861596

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026