Effect of Samples on Acne Treatment With Epiduo® Gel
Completed · Phase 4
Conditions studied: Acne Vulgaris
In brief
The purpose of this study is to compare adherence to treatment and efficacy with Epiduo® Gel in patients with mild to moderate acne who receive a medication sample and instructions on proper application with their stock size medication tube versus patients who receive only the stock size medication tube.
Key facts
- Study ID
- NCT01504204
- Run by
- Wake Forest University
- People needed
- 20
- Starts
- 2011-12-01
- Expected to finish
- 2012-11-01
- Last updated by the study team
- 2018-09-12
Who can join
Age: 12 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Male or female subject with mild to moderate acne, aged 12 and older, who agrees to participate and provides written consent.
- Have an Acne Global Assessment (AGA) of mild to moderate acne (an AGA score of 2 or 3)
You may not qualify if…
- Presence of a concurrent medical condition or skin condition, which is determined by the investigator to potentially interfere with study outcomes or patient assessments.
- Subjects with known allergy or sensitivity to Epiduo® Gel (or Benzoyl Peroxide Gel) or components therein, including adapalene or benzoyl peroxide
- Female subjects who are not postmenopausal for at least 1 year, surgically sterile, or willing to practice effective contraception during the study. Reliable methods of birth control are: abstinence (not having sex), oral contraceptives, intrauterine device (IUD), Depo-Provera, tubal ligation, or vasectomy of the partner (with confirmed negative sperm counts) in a monogamous relationship (same partner). An acceptable, although less reliable, method involves the careful use of condoms and spermicidal foam or gel and/or a cervical cap or sponge. Nursing mothers, pregnant women and women planning to become pregnant while on study are to be excluded.
Where it is running
- Wake Forest University Health Sciences — Winston-Salem, North Carolina, United States
Full record on ClinicalTrials.gov
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