Clinical Trials Directory

Trials / Unknown

UnknownNCT01111994

Efficacy & Safety of Clindamycin and Tretinoin in Acne

Efficacy & Safety of Clindamycin Phosphase 1.2% and Tretinoin 0.025% Gel vs. Vehicle for the Treatment of Acne and Acne-Induced Post Inflammatory Hyperpigmentation in Patients With Skin of Color

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
30 (estimated)
Sponsor
Callender Center for Clinical Research · Academic / Other
Sex
All
Age
12 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is ascertain the efficacy and safety of Clindamycin Phosphate 1.2% and Tretinoin 0.025% in the treatment of Acne and Post Inflammatory Hyperpigmentation in patients with skin of color.

Detailed description

Acne is a chronic disorder of the pilosebaceous glands characterized by inflammatory papules, pustules, opened and closed comedones, cysts and nodules. Post inflammatory hyperpigmentation is a condition in which an inflammation from a disease such as acne, trauma, or abrasion results in areas of the skin with increased melanin content compared to the surrounding skin. There are several treatments available for acne, which include benzoyl peroxide,antibiotics (topical or oral), and topical retinoids (tretinoin, tazarotene, adapalene). Combination therapy, such as topical retinoid and clindamycin, has been shown to be more effective than monotherapy in addressing all pathogenic factors of acne.

Conditions

Interventions

TypeNameDescription
DRUGClindamycin Phosphate 1.2% and Tretinoin 0.025% GelClindamycin Phosphate 1.2% and Tretinoin 0.025% Gel QD for 3 months

Timeline

Start date
2009-11-01
Primary completion
2010-03-01
Completion
2010-04-01
First posted
2010-04-28
Last updated
2010-05-20

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01111994. Inclusion in this directory is not an endorsement.