A Novel Method to Improve Acne Outcomes

Completed · Not applicable

Conditions studied: Acne Vulgaris

In brief

This is an investigator-blinded, prospective study of 20 subjects aged 13 through 18 with mild to moderate acne. Study subjects will be randomized to an internet survey group, in which an email link for a survey ascertaining the status of the subject's acne is sent weekly, or to a control group. All study subjects will use benzoyl peroxide 5% gel, and adherence and clinical improvement will be monitored over 12 weeks. The investigators hypothesis is that subjects in the internet survey group will have improved adherence to the study medication and clinical outcomes, because the weekly survey will remind subjects to use their medication.

Key facts

Study ID
NCT01176955
Run by
Wake Forest University
People needed
20
Starts
2009-05-01
Expected to finish
2010-08-01
Last updated by the study team
2018-08-16

Who can join

Age: 13 and older, up to 18. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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