Adherence to Study Medication Compared to Generic Topical Clindamycin Plus Generic Topical Tretinoin in Subjects With Mild to Moderate Acne Vulgaris
Phase 4
Completed
- Conditions
- Acne Vulgaris
- Interventions
- Registration Number
- NCT01047189
- Lead Sponsor
- Wake Forest University
- Brief Summary
The purpose of this research study is to evaluate the effectiveness of two different types of topical acne medication. This study will help to determine if one combined medication results in better acne improvement than two separate medications for acne.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 26
Inclusion Criteria
- Males or Females 12 years of age or older with a diagnosis of mild to moderate acne vulgaris.
- Subjects must sign written informed consent and agree to come for all study visits.
Exclusion Criteria
- Use of experimental drugs within 1 month prior to initiation of study therapy.
- Pregnant and nursing females will not be allowed in the study, and females of childbearing potential will have a pregnancy test at baseline. Females of childbearing potential must agree to use approved birth control methods for the duration of the study.
- Use of systemic retinoids within 2 months of enrollment, use of any topical retinoids, systemic antibiotics, nicotinamide, systemic steroids or any other medication that may confound the results of the study within 1 month prior to start of the study
- Use of any other topical medications for acne, including cosmetics containing retinol, within 2 weeks prior to study entry.
- Any skin condition or disease that may require concurrent therapy or may confound the evaluation;
- History of hypersensitivity to any of the formulation components;
- Facial skin cancer or facial actinic keratosis;
- Use of any photosensitizing agents.
- Use of isotretinoin within the last 6 months.
- Chemical peels, microdermabrasion or laser resurfacing within 3 months of study entry.
- Crohns disease, ulcerative colitis, or have developed colitis with past antibiotic use.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description 1 clindamycin phosphate 1.2% and tretinoin 0.025% Ziana gel (clindamycin phosphate 1.2% and tretinoin 0.025%) applied once daily for 12 weeks 2 clindamycin 1% gel Generic clindamycin 1% gel plus tretinoin 0.025% cream 2 tretinoin 0.025% cream Generic clindamycin 1% gel plus tretinoin 0.025% cream
- Primary Outcome Measures
Name Time Method Measured Adherence to ZIANA Gel or Generic Topical Clindamycin 1% Gel Each Morning Plus Generic Topical Tretinoin 0.025% Cream Each Evening in Subjects With Mild to Moderate Acne 12 weeks Percentage of prescribed doses taken as measured by a Medication Event Monitoring System (MEMS) cap
- Secondary Outcome Measures
Name Time Method The Change (Dynamic Assessment) From Baseline to Week 12 (or End of Treatment) in Total Acne Lesion Count Baseline to 12 weeks
Trial Locations
- Locations (1)
Wake Forest University Health Sciences, Dermatology
🇺🇸Winston-Salem, North Carolina, United States