Open-Label Pilot Study of the Efficacy and Safety of Vusion Ointment for the Treatment of Intertrigo
Completed · Early Phase 1
Conditions studied: Intertrigo
In brief
The purpose of this study is to determine if people with moist, red, patches on their skin in body folds would benefit treatment of those areas with an FDA-approved drug called Vusion.
Key facts
- Study ID
- NCT01118910
- Run by
- Image Dermatology P.C.
- People needed
- 15
- Starts
- 2010-04-01
- Expected to finish
- 2011-05-01
- Last updated by the study team
- 2011-08-04
Who can join
Age: 12 and older, up to 75. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Evidence of intertrigo
You may not qualify if…
- Pregnancy
- Use of systemic or topical antifungal or corticosteroid treatment in the previous 14 days or during the 3-month treatment period
- allergy of sensitivity to Vusion
- undergoing warfarin anticoagulation
- alcohol or drug abuse
- Investigator determines they cannot particpate
- history of non-compliance or poor cooperation
- participation in an investigaitonal drug study within 30 days of Baseline Visit
Where it is running
- Image Dermatology P.C. — Montclair, New Jersey, United States
Full record on ClinicalTrials.gov
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