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Comparison of Microneedling with Metformin Cream and Microneedling with Glutathione Cream in Reducing Dark Facial Patches (Melasma) in Adult

A Study On Efficacy Of Microneedling With Topical Metformin Versus Microneedling With Topical Glutathione In Treatment Of Melasma A Randomized Controlled Study - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/105051
Enrollment
60
Registered
2026-02-27
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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: Microneedling With Topical Metformin: Topical metformin cream containing metformin hydrochloride fifteen grams in one hundred grams of cream base liquid paraffin twenty five grams beesw

Sponsors

Dr YASHASWINI G S
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Female patients aged twenty to fifty years with clinically diagnosed facial melasma Fitzpatrick skin type three or four willing to give informed consent and comply with study protocol and not receiving any melasma treatment for at least three months prior to enrollment

Exclusion criteria

Exclusion criteria: Patients who are pregnant or breastfeeding Females with PCOD Smokers Active hormonal therapy Consumption of antioxidants in last Three months Use of isotretinoin in past six months Active inflammatory acne lesions Drugs causing photosensitivity and hyperpigmentation as epileptic drugs Antimilaria and tetracycline

Design outcomes

Primary

MeasureTime frame
Change in modified Melasma Area And Severity Index score from baseline to the end of treatment in each group and comparison of mean percentage reduction in modified Melasma Area And Severity Index between microneedling with topical metformin and microneedling with topical glutathioneTimepoint: 4 weeks & 8 weeks

Secondary

MeasureTime frame
Change in Global Photographic Assessment score & documentation of treatment related adverse effects & patient satisfaction in both groupsTimepoint: 4 weeks & 8 weeks

Countries

India

Contacts

Public ContactDr Yashaswini G S

Sri Devaraj Urs Medical College

Rajashekardermat@sduaher.ac.in9448316136

Outcome results

None listed

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