Comparing the treatment effect of microneedling with topical retinoid in patients with comedonal acne
Not Applicable
Recruiting
- Conditions
- acne.acne vulgaris
- Registration Number
- IRCT20140624018210N7
- Lead Sponsor
- Iran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 82
Inclusion Criteria
All patients having comedonal acne with any age and sex
Exclusion Criteria
Patients having inflamatory and severe acne/Patients under treatment with systemic drugs against acne
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Acne severity. Timepoint: Cases:every two weeks during treatment and 3 month after treatment cessation/Controls:every month during treatment and 3 months after treatment cessation. Method of measurement: Subjective assesment by the patient and with a questionnaire/objective assesment by the physician and based on acne severity index.
- Secondary Outcome Measures
Name Time Method