A comparison of the success rate of pneumatic reduction in intussusception between general anesthesia and deep sedation,A randomized controlled trial

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

TCTR

Registry ID

TCTR20190519001

Enrollment

Registered

2019-05-19

Start date

2019-05-01

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

Intussusception Intussusception Sedation Reduction General Anesthesia

Interventions

General Anesthesia as Protocol,Deep Sedation as Protocol

Active Comparator Procedure/Surgery,Active Comparator Procedure/Surgery

General Anesthesia,Deep Sedation

Eligibility

Sex/Gender

All

Age

0 Years to 15 Years

Inclusion criteria

Inclusion criteria: Intussusception patient at age 0-15 yr. who was treated with pneumatic reduction under fluoroscopic guidance in Division of Pediatric Surgery, Department of surgery, Chiang Mai university hospital

Exclusion criteria

Exclusion criteria: - Peritonitis - Nonresponsive shock - Perforation sign on radiographic study

Design outcomes

Primary

Measure	Time frame
Successful of non-surgical reduction 1-3 days within admission Categorical	—

Secondary

Measure	Time frame
Reduction complication and time to reduction 1-3 days within admission Categorical, Continuous	—

Contacts

Public ContactJiraporn Khorana

Faculty of Medicine, Chiang Mai University

jiraporn.kho@elearning.cmu.ac.th66819929767

Outcome results

None listed

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

A comparison of the success rate of pneumatic reduction in intussusception between general anesthesia and deep sedation&#44;A randomized controlled trial