Effect of topical ointment losartan versus placebo ointment on improvement of surgical scar

Phase 3

Recruiting

• Conditions: Surgical scar.; Scar conditions and fibrosis of skin; L90.5

• Registration Number: IRCT20120215009014N453
• Lead Sponsor: Hamedan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 7 February 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

Age 18 to 70 years
Age 18 to 70 years

Exclusion Criteria

Pregnancy or breastfeeding
The presence of a wound or infection at the treatment site
Coagulation disorder or immune system disorder

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Improvement of surgical scar. Timepoint: 6 weeks and 3 months after treatment. Method of measurement: Using Vancouver scar scale.