Examining the benefits of combination treatment in acne

Not Applicable

• Conditions: Atrophic acne scars.; Acne vulgaris; L70.0

• Registration Number: IRCT20230725058916N1
• Lead Sponsor: Shahid Beheshti University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 21 August 2023

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 25

Inclusion Criteria

Adult patients with atrophic rolling acne scars

Exclusion Criteria

Active acne
Active bacterial or viral infections
Bleeding disorders
Current use of systemic retinoids or during the last year
Hypertrophic scars
Hypersensitivity to anesthesia drugs

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Atrophic scar improvement. Timepoint: One and three months after treatment. Method of measurement: Comparison of photos before and after treatment, comments of the patient and the attending physicians (2 physicians) (Goodman and Baron's acne scar grading system).