Comparison of efficacy of subcision using blunt canula and nokor
Not Applicable
- Conditions
- Acne scar.Scar conditions and fibrosis of skin
- Registration Number
- IRCT2017082927707N2
- Lead Sponsor
- Vice-Chancellor in research Affairs of Shahid Beheshti University of Medical Science
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 35
Inclusion Criteria
inclusion criteria: patients with atrophic acne scar (rolling type); the range of age betwwen 18 to 65
exclusion criteria: pregnancy; autoimmune connective tissue disorder; cronary artery disease; coagulopathy; local infection; history of hayper trophic scar; inflamtory cutaneous disorders (psoriasis,lichen planus)
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Acne scar. Timepoint: Before intervention, 1 and 3 month after intervention. Method of measurement: Objective.
- Secondary Outcome Measures
Name Time Method Edema. Timepoint: 1 and 3 month after intervention. Method of measurement: Observation.;Echymose. Timepoint: 1 and 3 month after intervention. Method of measurement: Observation.;Nodule. Timepoint: 1 and 3 month after intervention. Method of measurement: Observation.