An A Study Assessing Subject Satisfaction With A-101 Topical Solution for Seborrheic Keratoses
Status: | Completed |
---|---|
Conditions: | Dermatology |
Therapuetic Areas: | Dermatology / Plastic Surgery |
Healthy: | No |
Age Range: | 30 - 65 |
Updated: | 2/27/2019 |
Start Date: | March 21, 2018 |
End Date: | November 14, 2018 |
An Open-Label Study Assessing Subject Satisfaction With A-101 Hydrogen Peroxide Topical Solution, 40% (w/w) Treatment for Seborrheic Keratoses of the Face, Neck, and Decolletage
This study is an open-label study designed to evaluate subject's satisfaction after treatment
of seborrheic keratoses with A-101 40%.
of seborrheic keratoses with A-101 40%.
Inclusion Criteria:
1. Subject can comprehend and is willing to sign an informed consent for participation in
this study.
2. Male or female between the ages of 30 and 65 years old.
3. Subject has 3 eligible Seborrheic Keratoses; 2 target SKs must be on the face, and the
additional 1 target SK must be on the neck or decolletage.
4. Subjects must have had cryosurgery for SK removal within the last 3 months and prior
to first treatment with A-101 Topical Solution.
5. Target and non-target SKs must not have been previously treated.
6. Subject is in good general health and free of any known disease state or physical
condition which, in the investigator's opinion, might impair the evaluation of any
target or non-target SK or which exposes the subject to an unacceptable risk by study
participation
Exclusion Criteria:
1. Subject has clinically atypical and /or rapidly growing Seborrheic Keratoses.
2. Subject has current systemic malignancy.
3. Subject would require the use of any topical treatment (e.g., moisturizers,
sunscreens) to any of the target or non-target SKs 12 hours prior to any study visit.
4. Subject has any current skin disease (e.g., psoriasis, atopic dermatitis, eczema, sun
damage), or condition (e.g., sunburn, excessive hair, open wounds) that, in the
opinion of the investigator, might put the subject at undue risk by study
participation or interfere with the study conduct or evaluations
We found this trial at
3
sites
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