Comparative Efficacy of Resveratrol 1 % Gel and Trichloroacetic Acid 20% in Treatment of Melasma: A Split-face Study

ConditionMelasma
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-50
SponsorAssiut University

About this trial

1. To evaluate the efficacy and safety of topical resveratrol 1 % gel in treatment of melasma. 2. To compare between the efficacy of topical resveratrol 1 %gel versrs chemical peeling with TCA 20% in melasma.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

• Age: 18-50 years old.

Pattern of melasma: Bilateral symmetrical facial melasma of any pattern.

Fitzpatrick skin phototypes: Types III, IV and V.

Disqualifiers

Pregnancy and lactation.

Patients taking oral contraceptive pills, hormonal replacement therapy or treatment for chronic illness at the time of the study or during the past 6 months.

Coexistence of diseases associated with hyperpigmentation such as Addison disease.

History of Scarring and keloid tendency

Trial design

Design model

Parallel

Treatments tested in this trial

  • resveratrol 1 % gel

    Drug

    left side of face the patient will be given resveratrol 1 % gel once daily at night (Home use ).

  • TCA20%

    Drug

    left side of face the patient will be given resveratrol 1 % gel once daily at night (homThee use ).

Treatment groups

41 Participants
are divided into 2 treatment groups
Group A: Group AActive comparator 1 intervention
Group B: Group BActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

The primary outcome is the change in hemi-Melasma Area and Severity Index (hemi-MASI) score from baseline to one month after the end of treatment (follow-up)

assessed by clinical evaluation and photographic documentation. Clinical efficacy will be categorized as: Excellent response: \>75% decrease in hemi-MASI score Very good response: 50-75% decrease in hemi-MASI score Good response: 25-50% decrease in hemi-MASI score Poor response: \<25% decrease in hemi-MASI score

Time frame
3 months

Secondary outcomes

Other outcomes

Sponsors and contacts

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