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Comparison of the Efficacy of Intradermal injected Tranexamic Acid vs Hydroquinone cream in the Treatment of Melasma

Comparison of the Efficacy of Intradermal injected Tranexamic Acid vs Hydroquinone cream in the Treatment of Melasma

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180203038599N1
Enrollment
40
Registered
2018-03-26
Start date
2017-08-23
Completion date
Unknown
Last updated
2018-04-30

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

Conditions

Melasma. Chloasma

Interventions

Intervention 1: Intervention group 1: Right side face treated with intradermal 4 mg/ml tranexamic acid every other week for 12 weeks. Intervention 2: Intervention group 2: Right side face treated with

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Women at the range of 18 to 50 years old with symmetrical bilateral melasma who signature the letter of satisfaction

Exclusion criteria

Exclusion criteria: Pregnant and lactating women Oral contraceptive pill consumption in 12 months ago during RCT History of coagulopathy and thrombotic disorder Anticoagulant and antiepileptic drug consumption Sensitivity to tranexamic acid History of treatment for melasma during 1 month ago Active facial herpes simplex virus infection Facial wart `

Design outcomes

Primary

MeasureTime frame
Melasma area and severity index. Timepoint: Melasma area and severity index measured at base of trial and 4, 8, 12 and 22. Method of measurement: Melasma area and severity index score.

Secondary

MeasureTime frame
Patients satisfaction. Timepoint: Measuring of patient satisfaction in 8, 12 and 22 week of trial. Method of measurement: Satisfaction percentage questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Zeynalie

Ahvaz University of Medical Sciences

zeynalie.m@ajums.ac.ir+98 61 3392 4392

Outcome results

None listed

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