A prospective randomized double-blind study of silicone gel plus herbal extracts versus placebo in pre-sternal hypertrophic scar preventio

Phase 3

Recruiting

• Conditions: Median stenal wound; Median stenal wound, scar prevention, silicone gel plus herbal extracts

• Registration Number: TCTR20140501001
• Lead Sponsor: Research center, Faculty of Medicine, Khon Kaen University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2014-05-01
• Study Completion: 2014-10-31
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

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

Inclusion Criteria

Patients had median stenotomy wound in 1 month after operation

Exclusion Criteria

History of keloid

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Scar prevention 6 months Vancouver scar scale

Secondary Outcome Measures

Name	Time	Method
Scar prevention 6 month Photograph assessment