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Effectiveness and safety of oral and intralesional tranexamic acid in treatment of melasma

Comparison of clinical efficacy and safety of oral and intralesional tranexamic acid in treatment of melasma - OITAM

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/08/035350
Enrollment
40
Registered
2021-08-03
Start date
Unknown
Completion date
Unknown
Last updated
2022-11-21

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 Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: tranexamic acid: 20 patients will be given oral tranexamic acid 250 mg twice a day for 12 weeks and in 20 patients cycles of intradermal microinjection with tranexamic acid will be give

Sponsors

Department of Dermatology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients with clinical diagnosis of melasma. 2. Patients above the age of 18 years and below the age of 50 years.

Exclusion criteria

Exclusion criteria: 1. Patients with a history of bleeding disorders 2. Patient taking oral anticoagulants, hormonal drugs like estrogen, progesterone, oral contraceptive pills and other female hormonal analogues. 3. Patients with past history of thrombotic disease like DVT. 4. Patients with family history of thrombotic disease. 5. Patients with known allergy to tranexamic acid. 6. Pregnant and lactation mothers. 7. Patients using photosensitizing drugs such as nonsteroidal anti-inflammatory drugs, tetracycline, spironolactone, phenytoin, carbamazepine, use of other depigmenting oral or topical agents. 8. Patients with any other facial dermatoses. 9. Patients with a history of any treatment for melasma in the past 6 months. 10. Patients with significant systemic illness.

Design outcomes

Primary

MeasureTime frame
To compare the clinical efficacy of oral and intralesional tranexamic acid in treatment of melasma.Timepoint: at 4, 8 and 12 weeks than follow up at 16, 20 and 24 weeks

Secondary

MeasureTime frame
NOT APPLICABLETimepoint: NOT APPLICABLE

Countries

India

Contacts

Public ContactDR GP THAMI

Govt Medical College and Hospital

thamigp@gmail.com9646121544

Outcome results

None listed

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