SkinCeuticals Discoloration Defense

Efficacy

Outcome				Grade		Effect		Evidence		Studies
Skin Smoothness				D		Potential Increase		Some		1 study 55 participants
Melasma				D		Potential Decrease		Some		1 study 48 participants
Hyperpigmentation				D		Potential Decrease		Some		1 study 55 participants
Skin Redness				E		No Effect		Some		1 study 55 participants

Mechanisms

Outcome				Grade		Effect		Evidence		Studies
Melanin				D		Potential Decrease		Some		1 study 55 participants

Side Effects

Outcome			Effect		Frequency			Studies
Itching			Increase		4% (2 out of 55 participants)			1 study
Pain			Increase		2% (1 out of 55 participants)			1 study
Skin Redness			Increase		5% (3 out of 55 participants)			1 study

1 Study Found

Intervention	SkinCeuticals Discoloration Defense
Concern	Skin Smoothness
Subject Type	Human
Trial Design	Non-Randomised Uncontrolled
Trial Duration	84 days
Participants	55

1 Study Found

Intervention	SkinCeuticals Discoloration Defense
Concern	Melasma
Subject Type	Human
Trial Design	Non-Randomised Uncontrolled
Trial Duration	84 days
Participants	55

1 Study Found

Intervention	SkinCeuticals Discoloration Defense
Concern	Hyperpigmentation
Subject Type	Human
Trial Design	Non-Randomised Uncontrolled
Trial Duration	84 days
Participants	55

1 Study Found

Intervention	SkinCeuticals Discoloration Defense
Concern	Skin Redness
Subject Type	Human
Trial Design	Non-Randomised Uncontrolled
Trial Duration	84 days
Participants	55

1 Study Found

Intervention	SkinCeuticals Discoloration Defense
Concern	Melanin
Subject Type	Human
Trial Design	Non-Randomised Uncontrolled
Trial Duration	84 days
Participants	55

1 Study Found

Intervention	SkinCeuticals Discoloration Defense
Concern	Itching
Subject Type	Human
Trial Design	Non-Randomised Uncontrolled
Trial Duration	84 days
Participants	55

1 Study Found

Intervention	SkinCeuticals Discoloration Defense
Concern	Pain
Subject Type	Human
Trial Design	Non-Randomised Uncontrolled
Trial Duration	84 days
Participants	55

1 Study Found

Intervention	SkinCeuticals Discoloration Defense
Concern	Skin Redness
Subject Type	Human
Trial Design	Non-Randomised Uncontrolled
Trial Duration	84 days
Participants	55

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