A randomized, double-blind, vehicle-controlled study of a preparation containing undecylenoyl phenylalanine 2% in the treatment of solar lentigines

Study Design

Subject Type

Human

Trial Design

Double-Blind, Randomised, Controlled

Trial Duration

84 days

Participants

36 (30 completed)

Age Range

47-75 years

Efficacy

Intervention(s)			Outcome		Method		Effect	Description
Undecylenoyl Phenylalanine			Hyperpigmentation		Counting		🠫	Sign in to read for free
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Side Effects

Intervention(s)	Outcome	Effect	Description
Undecylenoyl Phenylalanine	Itching	⇧	Sign in to read for free
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Undecylenoyl Phenylalanine	Skin Discomfort	⇧	Sign in to read for free
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Undecylenoyl Phenylalanine	Skin Redness	⇧	Sign in to read for free
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Study Summary