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Quassia Extract
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Efficacy
Outcome
Grade
Effect
Evidence
Studies
Rosacea
D
Potential Decrease
Some
1 study
27 participants
Spider Veins
D
Potential Decrease
Some
1 study
27 participants
Skin Redness
D
Potential Decrease
Some
1 study
27 participants
1 Study Found
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Evaluation of the efficacy and tolerance of a topical gel with 4% quassia extract in the treatment of rosacea
Intervention
Quassia Extract
Concern
Rosacea
Subject Type
Human
Trial Design
Open-Label
Non-Randomised
Uncontrolled
Trial Duration
45 days
Participants
30
See study summary and outcomes
1 Study Found
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Evaluation of the efficacy and tolerance of a topical gel with 4% quassia extract in the treatment of rosacea
Intervention
Quassia Extract
Concern
Spider Veins
Subject Type
Human
Trial Design
Open-Label
Non-Randomised
Uncontrolled
Trial Duration
45 days
Participants
30
See study summary and outcomes
1 Study Found
Close menu
Evaluation of the efficacy and tolerance of a topical gel with 4% quassia extract in the treatment of rosacea
Intervention
Quassia Extract
Concern
Skin Redness
Subject Type
Human
Trial Design
Open-Label
Non-Randomised
Uncontrolled
Trial Duration
45 days
Participants
30
See study summary and outcomes
Latest Research
Evaluation of the efficacy and tolerance of a topical gel with 4% quassia extract in the treatment of rosacea (2012)
See study outcomes
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