Prevention of Unfavorable Scars by Silicone Gel

Phase 4

Active, not recruiting

• Conditions: scar quality; scar; hypertrophic scar; keloid; silicone; silicone get

• Registration Number: TCTR20160904001
• Lead Sponsor: ond Rojvachiranonda

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2016-09-04
• Study Completion: 2017-11-25
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Active, not recruiting
• Sex: Female
• Target Recruitment: 24

Inclusion Criteria

Pregnant women who receive cesarean section via Pfannenstiel incision

Exclusion Criteria

1. intends to use scar product(s) to prevent unfavourable scar after the cesarean section
2. uses any other scar product(s) not in the protocol
3. there is wound disruption
4. there is wound infection
5. has chronic illness or condition that affects wound healing such as diabetes, hypertension, steroid user
6. cannot have up to one year of follow up

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
scar quality 2, 6, 12 months physical examination, photography, Vancouver and visual scar scales

Secondary Outcome Measures

Name	Time	Method
side effects 2 months, 6 months, 12 months history taking, physical examination, photography