Comparison of intussusception reduction time in pneumatic reduction between with and without balloon in pediatric ileocolic intussusception: a randomized trial

Status

Recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

TCTR

Registry ID

TCTR20250220003

Enrollment

Registered

2025-02-20

Start date

2025-02-13

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

Intussusception Intussusception Ileocolic Pneumatic reduction Fluoroscopy

Interventions

The Foley is insufflated 10 ml before starting pneumatic reduction,No balloon is used

Active Comparator Procedure/Surgery,No Intervention Procedure/Surgery

Balloon,No balloon

Eligibility

Sex/Gender

All

Age

1 Days to 7 Years

Inclusion criteria

Inclusion criteria: 1. Age less than 7 years old 2. Ultrasonographic diagnosis of ileocolic intussusception by radiology residents or a pediatric radiologist 3. Guardian consent to participate in the research project.

Exclusion criteria

Exclusion criteria: 1. Presence of pneumoperitoneum in abdominal radiographs reviewed by a pediatric radiologist 2. Sign of peritonitis from physical examinations determined by surgeons 3. Unstable vital signs for age groups

Design outcomes

Primary

Measure	Time frame
Reduction time end of procedure second	—

Secondary

Measure	Time frame
success rate end of procedure yes/no,complication end of procedure present	—

Countries

Thailand

Contacts

Public ContactWipawee Morakote

Faculty of Medicine, Chiang Mai University

wipawee.m@cmu.ac.th0869219493

Outcome results

None listed

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