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

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

TCTR

Registry ID

TCTR20140501001

Enrollment

Registered

2014-05-01

Start date

2013-09-24

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

Median stenal wound Median stenal wound&#44

Interventions

Apply scar twice daily,Apply scar twice daily

Active Comparator Drug,Placebo Comparator Drug

Silicone gel plus herbal extracts,Placebo

Eligibility

Sex/Gender

All

Age

15 Years to 70 Years

Inclusion criteria

Inclusion criteria: Patients had median stenotomy wound in 1 month after operation

Exclusion criteria

Exclusion criteria: History of keloid

Design outcomes

Primary

Measure	Time frame
Scar prevention 6 months Vancouver scar scale	—

Secondary

Measure	Time frame
Scar prevention 6 month Photograph assessment	—

Countries

Thailand

Contacts

Public ContactPolasak Jeeravipoolvarn

Khon Kaen University Ethics Committee in Human Research

medres@kku.ac.th043-363355

Outcome results

None listed

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

A prospective randomized double&#45;blind study of silicone gel plus herbal extracts versus placebo in pre&#45;sternal hypertrophic scar prevention