Efficacy/Safety/Subject Satisfaction/Duration of Response of Clobetasol Propionate Spray vs Ointment in Plaque Psoriasis
Completed · Phase 4
Conditions studied: Plaque Psoriasis
In brief
This study is a comparison between Clobetasol Propionate Spray and Clobetasol Propionate Ointment with Regard to Efficacy, Safety, Subject Satisfaction and Duration of Response in Moderate to Severe Stable Plaque Psoriasis. Subjects will be enrolled and randomized into one of two groups: clobetasol propionate Spray for 4 weeks of treatment or clobetasol propionate ointment for 2 weeks of treatment with a 2 week follow-up visit for each group.
Key facts
- Study ID
- NCT00733954
- Run by
- Galderma R&D
- People needed
- 250
- Starts
- 2007-08-01
- Expected to finish
- 2008-04-01
- Last updated by the study team
- 2022-08-23
Who can join
Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Subjects with a diagnosis of moderate to severe plaque psoriasis, defined as 3% - 20% of the body surface area. For the purposes of study treatment, most areas will be treated with the exception of face, scalp, groin, axillae and other intertriginous areas
- Overall disease severity is at least 3 (moderate)
You may not qualify if…
- Subjects who have surface area involvement too large that would require more than 50 grams per week of clobetasol propionate spray or more than 50 grams per week of clobetasol propionate ointment
- Subjects whose psoriasis involves only the scalp, face or groin
- Subjects with non-plaque psoriasis or other related diseases not classified as plaque psoriasis
Where it is running
- East Bay Dermatology Medical Group, Inc. — Fremont, California, United States
- Solano Clinical Research — Vallejo, California, United States
- Henry Ford Medical Center — Detroit, Michigan, United States
- Minnesota Clinical Study Center — Fridley, Minnesota, United States
- Dermatology Associates of Rochester — Rochester, New York, United States
- Baylor Research Institute - Dermatology Research — Dallas, Texas, United States
Full record on ClinicalTrials.gov
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