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ABSTRACT: Objectives
The primary aim of this study was to assess the change in acne lesions and severity within all treatment groups over the course of a six-month study.Methods
This was a six-month, multisite, randomized, double-blind, controlled study in female subjects with mild-to-moderate acne to assess the clinical and psychological outcomes of treatment with biofilm disrupting acne cream 2x, biofilm disrupting acne cream 1x, biofilm disrupting acne cream without salicylic acid, 2.5% benzoyl peroxide (BPO) gel, and placebo. Subjects applied the assigned product to their face twice daily and were evaluated for clinical acne and quality of life outcomes at baseline and after six, 12, 18, and 24 weeks of treatment.Results
After 24 weeks of use, subjects treated with biofil
SUBMITTER: Marshall-Hudson A
PROVIDER: S-EPMC10110293 | biostudies-literature | 2023 Apr
REPOSITORIES: biostudies-literature