FindTrial
Sign In

The comparison of sternal closure material in postoperative pectus deformities in pediatric congenital heart surgery, a randomized controlled trial.

Effect of materials in sternal closure : a randomised controlled trial

Status
Recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20200508004
Enrollment
60
Registered
2020-05-08
Start date
2019-11-01
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

Pectus deformities

Interventions

Ticron suture no. 0 and 2&#45
0,Stainless steel monofilament material
Experimental Device,Experimental Device
Ticron,Sternal wire

Sponsors

Research division, Faculty of medicine Siriraj hospital, Mahidol university, Thailand
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Months to 5 Years

Inclusion criteria

Inclusion criteria: Children since birth until 5 year-old who plan to operate open heart surgery

Exclusion criteria

Exclusion criteria: Delayed primary closure

Design outcomes

Primary

MeasureTime frame
Pectus deformities preoperative, postoperative at 1 and 6 months Chest X-ray AP and lateral views—

Secondary

MeasureTime frame
Infection rate within 1 month postoperative Presence of infection—

Countries

Thailand

Contacts

Public ContactChanut Chatkaewpaisal

Cardiovascular thoracic surgery unit, Faculty of medicine Siriraj hospital

tide_sk@hotmail.com0847648764

Outcome results

None listed

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