Clinical outcomes following caudal analgesia in infants undergoing Kasai portoenterostomy: A 10-year retrospective cohort study

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

TCTR

Registry ID

TCTR20260114007

Enrollment

Registered

2026-01-14

Start date

2014-01-01

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

Biliary atresia Kasai portoenterostomy Postoperative pain Caudal epidural analgesia biliary atresia analgesia epidural portoenterostomy hepatic postoperative period

Interventions

Patients undergoing the Kasai portoenterostomy, who received caudal analgesia. ,Patients undergoing the Kasai portoenterostomy, who did not received caudal analgesia.

Other,Other

Caudal,No Caudal

Eligibility

Sex/Gender

All

Age

No minimum to 1 Years

Inclusion criteria

Inclusion criteria: 1. Infants diagnosed with biliary atresia. 2. Underwent Kasai portoenterostomy under general anesthesia at Srinagarind Hospital between 1 Jan 2014 and 31 Dec 2023. 3. Elective or emergency surgery included.

Exclusion criteria

Exclusion criteria: 1. Patients whose records did not contain sufficient documentation were excluded.

Design outcomes

Primary

Measure	Time frame
Postoperative pain score Day 0-3 Pain score	—

Secondary

Measure	Time frame
Intraoperative outcomes within 10 year hemodynamic stability,Postoperative outcomes Within 10 years Postoperative outcomes	—

Countries

Thailand

Contacts

Public ContactDarunee Sripadungkul

Khon Kaen University

daruneesripa@gmail.com0883223257

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026