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comparing two standard methods of diversion stoma creation in cases of diseases requiring resection of rectum

Diverting loop ileostomy versus loop colostomy in rectal resections : a randomised controlled trial - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/101162
Enrollment
60
Registered
2026-01-14
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Health Condition 1: K639- Disease of intestine, unspecified Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: Diversion Stoma in two arms: Ileostomy creation for diversion for rectal resections Control Intervention1: Diversion Stoma in two arms: Colostomy creation for diversion for rectal resec

Sponsors

Arunjeet KK
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients with any pathology requiring rectal resections with colorectal or coloanal anastomosis 2. Patients planned to be treated by covering stoma either loop ileostomy or transverse colostomy

Exclusion criteria

Exclusion criteria: 1. Obstructed and Perforated tumors 2. Patients with permanent colostomy or ileostomy 3. Technical inability to perform ileostomy or colostomy, for example, previous bowel resection or anatomical factors 4. Aged less than 18 years 5. Inability of the patient to adequately cooperate.

Design outcomes

Primary

MeasureTime frame
Occurrence of ileus or obstruction in immediate post operative period, due to clinically significant oedema measured using time to tolerating oral feeding and length of hospital stay.Timepoint: Occurrence of ileus or obstruction in immediate post operative period, due to clinically significant oedema measured using time to tolerating oral feeding and length of hospital stay.

Secondary

MeasureTime frame
1)Occurrence of any of the enumerated stoma related complications within 30 days from primary surgery, reported using the Comprehensive Complication Index (CCI) based on CDC 2) Occurrence of any of the enumerated stoma related complications within 30 days from stoma closure reported using CCI, given stoma closure occurred within 3 months of primary surgery Timepoint: anytime within 30 days;Tertiary objective: Occurrence of Incisional Hernia after Stoma Closure within 1 year of closure surgery Timepoint:

Countries

India

Contacts

Public ContactArunjeet KK

Aster Medcity

deepak.varma1@asterhospital.in9446023075

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026