Comparing the Effect of Benzoyl Proxide 5% and IPL andto Proxide 5%-alone in acne
Phase 2
Completed
- Conditions
- Acne vulgaris.Acne vulgaris
- Registration Number
- IRCT2016051727947N1
- Lead Sponsor
- Isfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 58
Inclusion Criteria
being afflicted with mild-to-moderate acne; patients who prefer to receive therapies faster than commonly used time-consuming treatments; having no acne scar; no pregnancy of breast feeding; consent to participate; receiving no antibiotic during past wo weeks or systemic steroid and retinoid during past 6 months; photosensitivity; no tendency to develop hyperthrophic scar;
Exclusion criteria: sensitivity to benzoyl peroxide; no regular visits; using co-treatments.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Acne Severity Index. Timepoint: Befor and 1, 2, 3 months after initiation and 1 month after the last visit. Method of measurement: Calculating corresponding formula based on the number of injuries.
- Secondary Outcome Measures
Name Time Method Acne Global Severity Scale. Timepoint: Before, 1,2,3 month after treatment and 1 month after final treatment. Method of measurement: Calculating corresponding formula based on the number of injuries.