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The Effectiveness of 3% Topical Tranexamic Acid Compared to 4% Topical Hydroquinone as Therapy of Melasma

The Effectiveness of 3% Topical Tranexamic Acid Compared to 4% Topical Hydroquinone as Therapy of Melasma

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06010810
Enrollment
20
Registered
2023-08-25
Start date
2023-06-01
Completion date
2023-09-30
Last updated
2023-09-21

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

Conditions

Melasma

Brief summary

The goal of this clinical trial is to compare 3% Topical Tranexamic Acid with 4% Topical Hydroquinone as Therapy of Melasma in Patients with Skin Type III-V. The main question\[s\] it aims to answer are: 1. Is there a greater decrease in mMASI score after application of 3% topical tranexamic acid compared to 4% hydroquinone in melasma patients with skin type III - V? 2. Is there a greater decrease in mexameter score after application of 3% topical tranexamic acid compared to 4% hydroquinone in melasma patients with skin type III - V? 3. Are there any side effects of topical therapy of 3% tranexamic acid cream on melasma patients with skin types III - V? Participants with melasma diagnostic will apply the tranexamic acid cream and hydroquinone cream on both sides of the face differently. Researchers will compare by measuring the mexameter score and mMasi score to see if there any decrease in both sides of the face.

Interventions

DRUG3 % Topical Tranexamic Acid

Patient will be given 3% Topical Tranexamic Acid, on half of the face, twice a day for 2 months

DRUG4% Topical Hidroquinone

Patient will be given 4% Topical Hidroquinone, on half of the face, twice a day for 2 months

Sponsors

Indonesia University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Female patients diagnosed with melasma. * 18-60 years old. * Fitzpatrick skin type III to V. * Willing to be a research subject (SP) and sign a consent sheet. research (informed consent).

Exclusion criteria

* Are pregnant and/or breastfeeding * History of taking hormonal contraceptives in the last 6 months * History of topical melasma therapy: corticosteroids, tretinoin, hydroquinone, and Another therapy that lightens the skin in the last 2 weeks. * Use oral systemic therapy or injection in melasma, such as oral acid tranexamic, oral antioxidant, vitamin C injection, and glutathione injection in 4 last week. * History of superficial peeling therapy in the last 4 weeks. * History of deep peeling, laser or mechanical abrasion therapy in the last 6 months. * Use drugs that are photosensitizers such as phenytoin, tetracycline, spironolactone, and carbamazepine. * History of bleeding disorders or being on blood-thinning therapy * Allergy to tranexamic acid * Difficulty in complying with treatment. * Are experiencing symptoms of COVID-19, such as fever, cough, sore throat, loss of sense of taste or smell, red eyes, diarrhea, rash on the skin

Design outcomes

Primary

MeasureTime frameDescription
Modified Melasma Area and Severity Index2 monthsDecrease of Modified Melasma Area and Severity Index
Mexameter score2 monthsDecrease of melanin index and erythema index

Countries

Indonesia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026