Clobetasol Propionate, 0.05%
DrugTopical, twice daily for 4 weeks
Other names: Clobex® Spray
NCT Number: NCT00437255
Evaluate the efficacy of Clobex® Spray as compared to Taclonex® Ointment in terms of Overall Disease Severity and Investigator Global Assessment.
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Notify Me18 year–80 year
All sexes
Interventional
Phase 4
Minnesota Clinical Study Center, Fridley, Minnesota, United States
Same as above.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Topical, twice daily for 4 weeks
Other names: Clobex® Spray
Topical, once daily
Other names: Taclonex® Ointment
Time frame: End of treatment (Week 4)
Time frame: Baseline, Weeks 1, 2, 4 and 8
Time frame: Weeks 1, 2 and 8
Time frame: End of treatment (week 4) and Weeks 1, 2 and 8
Galderma R&D
Industry
An Evaluation of the Efficacy, Safety, Preference and Duration of Response of Clobex® (Clobetasol Propionate) Spray and Taclonex® (Calcipotriene 0.05%/Betamethasone Dipropionate 0.064%) Ointment in Subjects With 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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