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A comparative study of microneedling versus intradermal injection using tranexamic acid in the treatment of Melasma

Efficacy of tranexamic acid microneedling versus intradermal injection of tranexamic acid in the treatment of Melasma-A Randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/05/052649
Enrollment
70
Registered
2023-05-15
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

Health Condition 1: L814- Other melanin hyperpigmentation

Interventions

Intervention1: Microneedling and Intradermal injection: Microneedling and Intradermal injection at monthly intervals 0,4,8,12 weeks Control Intervention1: Tranexamic acid micro needling and intraderma

Sponsors

AARUPADAI VEEDU MEDICAL COLLEGE,PONDICHERRY
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients with Epidermal/Dermal /Mixed type of melasma 2.Patients willing for consent, study and follow up

Exclusion criteria

Exclusion criteria: 1.Pregnancy 2,Patients on hormone replacement therapy 3.Patients on contraceptive pills 4.Patients on anticoagulants 5.Allergic to drugs under the study 6.Non compliant patients 7.Patients with keloidal or Hypertrophic scar tendency 8.Patients with the history of depigmenting treatment in the past 1 month 9.Moderate to severe acne vulgaris on face 10.History of Herpes infections, Warts

Design outcomes

Primary

MeasureTime frame
Modified Melasma Area and Severity Index (Modified MASI) score: Primary outcome to assess treatment response.Timepoint: At baseline,4weeks, 8weeks & 12 weeks and followed up for further 2 months at monthly intervals.

Secondary

MeasureTime frame
Clinical improvement assessed based on photographic documentTimepoint: At baseline, 4weeks, 8weeks & 12 weeks and followed up for further 2 months at monthly intervals. ;Patient global assessment scale andTimepoint: At baseline, 4weeks, 8weeks & 12 weeks and followed up for further 2 months at monthly intervals.

Countries

India

Contacts

Public ContactSRIJHA M

Aarupadai veedu medical college,Pondicherry

deepakaliyaperumal@gmail.com9488511884

Outcome results

None listed

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