Clinical trial test of the efficacy and safety of the decompression of the Liquid Balloon ILeus Tube in treatment of the Bowel obstruction

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2300075129

Enrollment

Unknown

Registered

2023-08-25

Start date

2018-09-29

Completion date

Unknown

Last updated

2023-08-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bowel obstruction

Interventions

Experimental group:Insertion of Liquid Balloon ILeus Tube

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) 18 years old = age =65 years old; (2) Inpatient with adhesive bowel obstruction or mechanical bowel obstruction; (3) Sign the 'Informed Consent Form'

Exclusion criteria

Exclusion criteria: (1) Mechanical Bowel obstruction caused by internal hernia, Volvulus, anastomotic stenosis, intestinal wall hematoma, etc; (2) Bowel obstruction requiring emergency surgery; (3) Suspected strangulating Bowel obstruction and blood circulation obstruction Bowel obstruction;(4) upper gastrointestinal bleeding; (5) esophageal varices; (6) Severe dysfunction of important organs;(7)Researchers believe that it is not appropriate to participate in this study

Design outcomes

Primary

Measure	Time frame
intubation success rate (passage through pylorus);	—

Secondary

Measure	Time frame
adverse event;Response rate of liquid and gas level on X-ray plain film in abdominal orthosis;First anal discharge (days);First anal exhaust rate;First bowel movement time (hours);First bowel rate;Transfer surgery rate;	—

Countries

China

Contacts

Public ContactYou Tao

The Second Affiliated Hospital of Wenzhou Medical University

814326792@qq.com+86 139 5770 6972

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026