Using metformin to treat melasma in Latin American women
Official title: Oral Metformin in the Treatment of Melasma: a Prospective Trial in Latin American Women
Run by University of Puerto Rico · NCT06845540 · Data updated 2026-11-12
This study is testing if the diabetes drug metformin can help reduce dark patches on the skin caused by melasma in Latin American women.
Quick facts
| Phase | Phase1; Phase2 |
|---|---|
| Study type | Interventional |
| Ages | 21 Years and up |
| Sex | Women only |
| Enrollment | 30 (estimated) |
| Sponsor | University of Puerto Rico Academic / other |
| Locations | 1 site (San Juan, PR) |
| Status | Recruiting |
| Started | February 20, 2025 |
| Main results expected | May 22, 2025 |
| Study ends | May 30, 2025 |
| Registry record updated | February 25, 2025 |
| Trial ID | NCT06845540 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are Latin American women aged 21 years or older with a diagnosis of epidermal or mixed melasma.
✕Probably not a fit
Patients who are pregnant, breastfeeding, or have a history of renal or liver disease will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This clinical trial aims to evaluate the effectiveness of metformin in reducing melasma in Latin American women. Participants will take either 500 mg or 1000 mg of metformin daily for three months. The study involves two clinic visits, one at the start and one at the end, along with follow-up phone calls to monitor progress and side effects. The primary focus is to determine if metformin can improve the appearance of dark patches associated with melasma.
Why it matters
Potential benefit: If successful, this treatment could provide a new option for women suffering from melasma, potentially improving their skin appearance and quality of life.
How similar studies have gone: While the use of metformin for melasma is a novel approach, other studies have explored its effects on skin conditions, but this specific application remains largely untested.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: Latin American women aged 21 years or older, diagnosed epidermal or mixed melasma Exclusion Criteria: pregnancy, breastfeeding, use of hydroquinone or tretinoin within 2 months before the study, or undergoing laser treatment, peels, microdermabrasion, or microneedling within 2 months of the study. Patients with a history of renal or liver disease, metformin allergy, diabetes, hypoglycemia, or those on medications that could interact with metformin will also be excluded.
Where it's running
-
Administración de Servicios Médicos (ASEM) Clinicas Externas
San Juan, Pr, Puerto Rico Recruiting
Study contacts
- Principal investigator: Cristina Brau — University of Puerto Rico
- Study coordinator: Cristina Brau
- Email: cbrau@skinbybrau.com
- Phone: 787-758-2525
Similar studies
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This study tests a depigmenting gel to see if it improves facial dark spots in 40 women aged 30–60 over 90 days.
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This trial will test whether using ultrasound to help the skin absorb a 10% tranexamic acid and 2% glutathione solution reduces facial melasma in adults aged 20–55.
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.