Comparative study of the efficacy between laparoscopic ileostomy reversal with intracorporeal anastomosis and standard ileostomy reversal

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100041632

Enrollment

Unknown

Registered

2021-01-01

Start date

2021-01-01

Completion date

Unknown

Last updated

2021-03-22

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

Conditions

Ileostomy status

Interventions

laparoscopic ileostomy reversal with intracorporeal:laparoscopic ileostomy reversal with intracorporeal anastomosis

standard ileostomy reversal:standard ileostomy reversal

Eligibility

Sex/Gender

All

Age

14 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients with ileostomy; 2. Patients who can tolerate laparoscopic surgery; 3. Patients and their families agree to laparoscopic surgery.

Exclusion criteria

Exclusion criteria: Nil

Design outcomes

Primary

Measure	Time frame
average hospitalization days ;the average operation time ;30-Day mortality rate;intraoperative blood loss;adhesion release rate;readmission rate;30 day complication rate;	—

Countries

China

Contacts

Public ContactYang Xiaobo

Department of gastrointestinal Surgery, The Second People's Hospital of Yibin

326232572@qq.com+86 13458471370

Outcome results

None listed

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