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.
Same as above.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
78
Apply to affected areas twice daily
Apply to affected areas twice daily
Solano Clinical Research
Vallejo, California, United States
Central Dermatology, PC
St Louis, Missouri, United States
Efficacy - Body Surface Area, Investigator Global Severity
Time frame: 6 weeks
Safety - Tolerability assessments, adverse events
Time frame: 6 weeks
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