Clobetasol Propionate 0.05% Spray
DrugApply to affected areas twice daily
Other names: Clobex® Spray
NCT Number: NCT00436540
The primary objective of this study is to evaluate the efficacy and safety of clobetasol propionate 0.05% (Clobex®) spray compared to clobetasol propionate 0.05% (Olux®) foam.
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Notify Me18 year–80 year
All sexes
Interventional
Phase 4
Solano Clinical Research, Vallejo, California, United States
Same as above.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Apply to affected areas twice daily
Other names: Clobex® Spray
Apply to affected areas twice daily
Other names: Olux® Foam
Time frame: 6 weeks
Time frame: 6 weeks
Galderma R&D
Industry
A Comparison Between Clobetasol Propionate (Clobex®) Spray and Clobetasol Propionate (Olux®) Foam With Regard to Efficacy, Safety, Preference and Duration of Response in Stable Plaque Psoriasis
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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