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

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

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.