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Clinical efficacy and safety of nano-microneedle-assisted phenylethyl resorcinol for the treatment of infraorbital dark circles
Study Design
Subject Type
Human
Trial Design
Single-Blind, Randomised, Controlled
Trial Duration
112 days
Participants
20
Age Range
20-50 years
Efficacy
Intervention(s)
Outcome
Method
Effect
Description
Phenylethyl Resorcinol
Skin Redness
Mexameter
–
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Phenylethyl Resorcinol
Under Eye Circles
Clinical grading
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Mechanisms
Intervention(s)
Outcome
Method
Effect
Description
Phenylethyl Resorcinol
Melanin
Mexameter
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Study Summary
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