Skip to content

Prevention of Unfavorable Scars by Silicone Gel

Prevention of Unfavorable Scars by Silicone Gel

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20160904001
Enrollment
Unknown
Registered
2016-09-04
Start date
2007-04-18
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

scar quality scar hypertrophic scar keloid silicone silicone get

Interventions

Silicone gel is applied to a half side of cesarian scar. The other side receive no treatment.
Experimental Other

Sponsors

Nond Rojvachiranonda
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Pregnant women who receive cesarean section via Pfannenstiel incision

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
scar quality 2, 6, 12 months physical examination, photography, Vancouver and visual scar scales

Secondary

MeasureTime frame
side effects 2 months, 6 months, 12 months history taking, physical examination, photography

Countries

Thailand

Contacts

Public ContactNond Rojvachiranonda

Chulalongkorn University

rnond@chula.ac.th+66897798283

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026