Trials / Completed
CompletedNCT00842153
Evaluation of the Efficacy and Tolerability of Clobetasol Propionate Foam Compared to Vehicle Foam
A Study to Evaluate the Efficacy and Tolerability of Clobetasol Propionate vs. Vehicle in the Treatment of Mild to Moderate Plaque-Type Psoriasis
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 58 (actual)
- Sponsor
- Stiefel, a GSK Company · Industry
- Sex
- All
- Age
- 12 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of the study is to compare the efficacy and safety of Clobetasol propionate to that of its Vehicle in the treatment of mild to moderate plaque-type psoriasis.
Detailed description
The purpose of the study is to compare the efficacy and safety of Clobetasol propionate to that of its Vehicle in the treatment of mild to moderate plaque-type psoriasis. This is a multi-center, double blind, randomized, parallel designed study which consists of 2 weeks of treatment and a follow-up visit 2 weeks later.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Clobetasol propionate foam | Topical Clobetasol propionate foam |
| DRUG | Vehicle foam | Vehicle foam does not include the active drug. |
Timeline
- Start date
- 2007-11-01
- Primary completion
- 2007-12-01
- Completion
- 2008-01-01
- First posted
- 2009-02-12
- Last updated
- 2017-10-09
- Results posted
- 2012-01-30
Locations
2 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT00842153. Inclusion in this directory is not an endorsement.