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Study identifier: NCT07071363 Synced from ClinicalTrials.gov · July 28, 2026
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COMPARISON OF A COSMETIC SERUM AND 4% HYDROQUINONE FOR TREATING MELASMA OVER 84 DAYS

Condition: Healthy · Melasma (Facial Melasma) · Epidermal Melasma  ·  Sponsor: Laboratoire Dermatologique ACM

PhaseNA
Planned participants40
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNo

About this study

The goal of this clinical trial is to compare the dermatological tolerance and skin-lightening efficacy of a cosmetic depigmenting serum to a 4% hydroquinone-based product in adult male and female subjects aged 18-65 years with mild to moderate epidermal or mixed-type melasma. The main questions it aims to answer are: Does the cosmetic serum reduce the severity of melasma (measured by mMASI) after 84 days of use? Is the cosmetic serum better tolerated than 4% hydroquinone under real-use conditions? Researchers will compare the serum group and the hydroquinone group to determine whether the cosmetic product achieves comparable pigmentation improvement with superior skin tolerability. Participants will: Group 1: Apply a morning routine (Depiwhite Serum + Depiwhite M SPF50+ cream) Apply an evening routine (Depiwhite Serum + Placebo Cream without Hydroquinone) Group 2: Apply a morning routine (Serum Placebo + Depiwhite M SPF50+ cream) Apply an evening routine (Serum Placebo + Depigmenting Cream with hydroquinone 4%) Visit the clinical site at baseline (Day 0), Day 56, and Day 84 for assessments Complete standardized photographs, self-assessment questionnaires, and quality-of-life surveys (MELASQoL and ASLQI) Undergo clinical evaluations by a dermatologist, including mMASI scoring and tolerance assessment

This description comes directly from the study's public registry record.

Talk to the study team

Dr Gitanjali PETKAR Principal Investigator (Dermatologist), (MBBS, DDV)  ·  +2304012600  ·  g.petkar@cidp-cro.com

Always discuss trial participation with your own doctor first.

Locations (1)

Centre International de Développement PharmaceutiquePort Louis, Phoenix, MauritiusRecruiting

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Source record: clinicaltrials.gov/study/NCT07071363