A Pilot, Multi-Center, Patient Preference Study Comparing Two Clindamycin/Benzoyl Peroxide Gels.
Phase 4
Completed
- Conditions
- Acne Vulgaris
- Registration Number
- NCT00377000
- Lead Sponsor
- Sanofi
- Brief Summary
Evaluate patient preference factors comparing two clindamycin/benzoyl peroxide gels. One dispensed in a pump presentation, the other in a tube presentation.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Not provided
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Exclusion Criteria
Not provided
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Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Primary Outcome Measures
Name Time Method Patient Preference Questionnaire evaluation: including product use, patient knowledge and impression of acne, as well as patient treatment The incidence of all adverse events reported during the study will be summarized by treatment group The signs and symptoms of irritation will be summarized descriptively by treatment group at every visit Investigator irritation grading - erythema, peeling, dryness and pruritus at Baseline (Week 0), Week 2, 4, and 6
- Secondary Outcome Measures
Name Time Method