跳至主要内容
临床试验/CTRI/2026/01/101162
CTRI/2026/01/101162尚未招募不适用

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

Arunjeet KK1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2026年1月31日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
60
试验地点
1

研究概览

简要总结

Diverting Loop Ileostomy versus Loop Colostomy in Rectal Resections(A Randomised Controlled trial)

Primary objective: 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 objective/s 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

Tertiary objective: Occurrence of Incisional Hernia after Stoma Closure within 1 year of closure surgery

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 99.00 Year(s)(—)
性别
All

入选标准

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

排除标准

  • Obstructed and Perforated tumors
  • Patients with permanent colostomy or ileostomy
  • Technical inability to perform ileostomy or colostomy, for example, previous bowel resection or anatomical factors
  • Aged less than 18 years 5.

研究者

发起方
Arunjeet KK
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Arunjeet KK

Aster Medcity

研究点 (1)

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