Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Narrows Institute for Biomedical Research
With
L'Oreal
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Men and women ages 18+.
Clinical diagnosis of Post Inflammatory Hyperpigmentation
Non-Caucasian
Fitzpatrick skin types IV-VI
Available and willing to comply with study instructions and attend all study visits.
Able and willing to provide written and verbal informed consent.
You may not be if
Subject has any skin pathology or condition that could interfere with the evaluation of the test products or requires the use of interfering topical or systemic therapy.
Caucasian/ Non-Hispanic
Subject has any condition which, in the investigator's opinion, would make it unsafe for the subject to participate in this research study.
Pregnant, lactating, or is planning to become pregnant during the study.
Subject is currently enrolled in an investigational drug or device study.
Subject has received an investigational drug or has been treated with an investigational device within 30 days prior to the initiation of treatment (baseline).
Study participant has facial hair that could interfere with the study assessments in the opinion of the investigator.
Study participant is unable to communicate or cooperate with the investigator due to language problems, poor mental development, or impaired cerebral function.
Subject has known hypersensitivity or previous allergic reaction to any of the active or inactive components of the test articles.
Subject has the need or plans to be exposed to artificial tanning devices or excessive sunlight during the trial.
