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Completed

NCT Number: NCT00823901

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

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

Department of Dermatology - Stanford School of Medicine, Stanford, California, United States

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About this study

Currently, there is no known cure for rosacea. The most effective treatment is systemic antibiotics, particularly of the tetracycline family. Topical treatments include metronidazole, antibacterials such as erythromycin and clindamycin, sulfacetamide and benzoyl peroxide. Isotretinoin (Accutane) is also used.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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.

Exclusion criteria

  • 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

Treatment and study plan

Clindamycin Phosphate 1.2% And Tretinoin 0.025% Gel

Drug

Applied on entire face (forehead, nose, cheeks, chin) once daily at night for 12 weeks

Other names: Ziana

Placebo Gel

Drug

Applied placebo gel with no active medication to entire face (forehead, nose, cheeks, chin) once daily at night for 12 weeks

Other names: placebo

Primary outcomes

  1. Mean Change in Number of Inflammatory Lesions From Baseline to Week 12

    Time frame: Baseline, week 12

    The number of inflammatory lesions (papules and pustules) on the face were counted by a dermatologist at baseline and week 12 for each participant. Change in the number of inflammatory lesions is defined as week 12 values minus the baseline values of the participant. Last observation carried forward (LOCF) method was used for missing values.

Sponsors and collaborators

Lead sponsor

Massachusetts General Hospital

Other

Collaborators

  • Medicis Pharmaceutical Corporation

Registry information

Official study title

A Double-Blind, Placebo-Controlled, Pilot Study to Determine the Safety and Efficacy of Clindamycin Phosphate 1.2% and Tretinoin 0.025% Gel For The Treatment of Rosacea Over 12 Weeks

Important dates

Study start
2009
Primary completion
2010
Study completion
2010
First posted
Jan 16, 2009
Registry last updated
Jun 25, 2012

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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