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Comparative study between topical hydroquinone 4% alone versus its combination with intradermal autologous platelet-rich plasma in the treatment of melasma: a split-face controlled trial

Phase 4
Recruiting
Conditions
Melasma
melasma, autologous platelet-rich plasma, hydroquinone
Registration Number
TCTR20210925002
Lead Sponsor
Institute of Dermatology
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
20
Inclusion Criteria

Otherwise healthy volunteers with Fitzpatrick skin type 2, 3, 4 who have melasma on both sides of cheeks, symmetrical or nearly symmetrical

Exclusion Criteria

Individuals who tend to develop keloid/acne or having active infection such as herpes, HIV, hepatitis, on oral isotretinoin or hormonal therapy within 6 months prior to this study, has a history of bleaching/whitening agents/laser therapy/botulinum toxin injection within 6 months or filler injection within 2 years prior to this study, pregnancy, lactation, smoking, bleeding tendency, facial dermatitis, skin malignancy or other skin conditions which might affect study results, on oral or topical antioxidants including vitamin C and whitening agents and those who has more than 3 hours of sun exposure per day.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Efficacy 2,4,6,8,12,16 weeks Biophysical properties of the skin, Clinical photographs
Secondary Outcome Measures
NameTimeMethod
Safety 2,4,6,8,12,16 weeks Patient satisfaction questionaire
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