A Washington University research study seeks female participants.
The purpose of this study is to determine if a study medication (topical cream) has beneficial effects and is safe for people with atopic dermatitis. Participants will be in the study for approximately 18 to 20 weeks. There are 8 study visits. There will be vital signs, EKG, lab tests, skin assessments, photography and an optional skin biopsy. Benefits and risks will be discussed with volunteers as part of the informed consent process. To compensate for your time, you will receive $50 for each completed visit for a total of up to $450 if you complete all visits (IRB # 201701074).
Nancy Bodet, RN:
Condition | Atopic Dermatitis |
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Clinical Study Identifier | TX151215 |
Last Modified on | 25 March 2021 |
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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