Safety and Efficacy Study of Clindamycin Phosphate 1.2% and Tretinoin 0.025% Gel to Treat Rosacea

Completed · Phase 2/Phase 3 · Has a placebo group

Conditions studied: Rosacea

In brief

The purpose of this study is to determine whether Clindamycin Phosphate 1.2% And Tretinoin 0.025% Gel are effective and safe in the treatment of papulopustular rosacea.

Key facts

Study ID

NCT00823901

Run by

Massachusetts General Hospital

People needed

83

Starts

2009-02-01

Expected to finish

2010-10-01

Last updated by the study team

2012-06-25

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects 18 years of age and older.
• Clinical diagnosis of papulopustular facial rosacea.
• A minimum of 4 but not more than 50 facial inflammatory lesions (papules plus pustules).
• Willing and able to understand and sign informed consent.
• Able to complete study and comply with study procedures.

You may not qualify if…

• Acne conglobata, acne fulminans, secondary acne (chloracne, drug-induced acne, etc.), or severe acne requiring systemic treatment.
• History or presence of regional enteritis or inflammatory bowel disease (e.g., ulcerative colitis, pseudomembranous colitis, chronic diarrhea, or a history of antibiotic-associated colitis, bloody diarrhea) or similar symptoms.
• Use of topical rosacea treatments in the past 2 weeks.
• Use of systemic antibiotics in the past 4 weeks.
• Use of systemic retinoids within the past 3 months.
• Use of laser or light based rosacea treatments within the past 2 months.
• Concomitant use of medications that are reported to exacerbate rosacea, such as topical and systemic steroids as these may impact assessments.
• Current drug or alcohol abuse.
• Other dermatologic conditions that require the use of interfering topical or systemic therapy or that might interfere with study assessments such as, but not limited to, atopic dermatitis, perioral dermatitis or acne vulgaris.
• Clinically significant abnormal findings or conditions (other than rosacea), which might, in the opinion of the Investigator, interfere with study evaluations or pose a risk to subject safety during the study.
• Subjects who are pregnant or planning a pregnancy.
• Use of any investigational therapy within the past 4 weeks.
• Known hypersensitivity or previous allergic reaction to clindamycin or retinoids

Where it is running

• Department of Dermatology - Stanford School of Medicine — Stanford, California, United States
• CURTIS - Massachussetts General Hospital — Boston, Massachusetts, United States

Full record on ClinicalTrials.gov

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