Comparison of the effects of triamcinolone and bleomycin on burn wounds

Phase 3

Recruiting

• Conditions: burn.; Calcification and ossification of muscles associated with burns; M61.3

• Registration Number: IRCT20120410009431N4
• Lead Sponsor: Iran 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: 35

Inclusion Criteria

Burn patients two months after recovery

Exclusion Criteria

Patient dissatisfaction
Hypersensitivity to triamcinolone or bleomycin

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Scar size. Timepoint: Four months after injection. Method of measurement: Using a ruler.;Pain in the injection area. Timepoint: After injection. Method of measurement: Visual Analogue Scale.

Secondary Outcome Measures

Name	Time	Method
Injection site inflammation. Timepoint: After injection. Method of measurement: Observation.