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临床试验/NCT07754227
NCT07754227已完成不适用

Comparison of Mean Post-Operative Hospital Stay in Early and Delayed Ileostomy Closure Following Bowel Surgery: A Randomized Controlled Trial

Dr. Waseem Ullah1 个研究点 分布在 1 个国家目标入组 73 人开始时间: 2026年1月2日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
73
试验地点
1
主要终点
Post-operative hospital stay

研究概览

简要总结

Temporary ileostomy is commonly created following bowel surgery to protect distal anastomoses and reduce the consequences of anastomotic leakage. However, the optimal timing for ileostomy closure remains controversial. Early closure may improve quality of life and reduce stoma-related complications, whereas delayed closure may allow better recovery but prolong stoma-related morbidity and hospital care. This randomized controlled trial aims to compare the mean post-operative hospital stay between early (within 8 weeks) and delayed (after 8 weeks) ileostomy closure following bowel surgery. Sixty eligible patients will be randomized equally into two groups. The findings will help determine the optimal timing of ileostomy reversal and may improve patient outcomes while reducing healthcare utilization.

详细描述

Temporary ileostomy is frequently performed after bowel surgery as a protective measure for intestinal anastomosis or as part of emergency surgical management. Although ileostomy closure is considered a routine procedure, the ideal timing of closure remains uncertain. Early closure has the potential to improve patient quality of life, reduce stoma-related complications, and shorten the overall treatment course. Conversely, delayed closure may provide additional time for recovery and anastomotic healing but may increase the duration of stoma-related morbidity and healthcare resource utilization.

This prospective, randomized controlled trial will be conducted in the Department of General Surgery, Lady Reading Hospital-Medical Teaching Institution, Peshawar, Pakistan. A total of 60 adult patients (18-65 years) with temporary ileostomy following bowel surgery who meet the eligibility criteria will be enrolled using consecutive sampling and randomized in a 1:1 ratio into two study groups using block randomization.

Participants in the intervention group will undergo early ileostomy closure within 8 weeks of ileostomy creation, while participants in the comparator group will undergo delayed ileostomy closure after 8 weeks. The primary outcome will be post-operative hospital stay, measured as the number of days from ileostomy closure surgery until hospital discharge.

Baseline demographic and clinical characteristics, including age, sex, body mass index, smoking status, hypertension, diabetes mellitus, residence, financial background, and post-operative complications, will be recorded. Data will be analyzed using IBM SPSS version 25. Continuous variables will be analyzed using the independent-samples t-test or Mann-Whitney U test according to data distribution, with statistical significance set at p < 0.05.

The study has received ethical approval from the Institutional Review Board of Lady Reading Hospital-Medical Teaching Institution, Peshawar (IRB Reference No. 85/LRH/MTI, dated 06 February 2025). The results are expected to provide evidence regarding the optimal timing of temporary ileostomy closure in terms of reducing post-operative hospital stay and improving clinical outcomes.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

盲法说明

This is an open-label surgical trial. Neither participants nor treating surgeons can be blinded because the timing of ileostomy closure is evident. Outcome assessment is based on objective hospital records.

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Adults aged 18-65 years.
  • •Male or female participants.
  • •Patients with a temporary ileostomy following bowel surgery.
  • •Patients scheduled for elective ileostomy closure.
  • •Participants willing to provide written informed consent.

排除标准

  • •Abdominal wall dehiscence.
  • •Tubercular perforation.
  • •Peritoneal contamination.
  • •Patients medically unfit for surgery.
  • •Refusal to provide informed consent.

研究组 & 干预措施

Early Ileostomy Closure

Experimental

Participants undergo ileostomy closure within 8 weeks of ileostomy creation following bowel surgery.

干预措施: Early Ileostomy Closure (Procedure)

Delayed Ileostomy Closure

Active Comparator

Participants undergo ileostomy closure more than 8 weeks after ileostomy creation following bowel surgery.

干预措施: Delayed Ileostomy Closure (Procedure)

结局指标

主要结局

Post-operative hospital stay

时间窗: From the date of ileostomy closure until hospital discharge (up to 30 days).

Post-operative hospital stay will be measured as the number of days from ileostomy closure surgery until discharge from the hospital. The mean duration will be compared between patients undergoing early (≤8 weeks) and delayed (\>8 weeks) ileostomy closure.

次要结局

未报告次要终点

研究者

发起方
Dr. Waseem Ullah
申办方类型
Other Gov
责任方
Sponsor Investigator
主要研究者

Dr. Waseem Ullah

Assistant Professor

Lady Reading Hospital, Pakistan

研究点 (1)

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