The Value of Bowel Sounds in Evaluating Postoperative Intestinal Function Recovery in Colorectal … (NCT07705139) | Clinical Trial Compass
RecruitingNot Applicable
The Value of Bowel Sounds in Evaluating Postoperative Intestinal Function Recovery in Colorectal Cancer Patients
China172 participantsStarted 2026-02-01
Plain-language summary
This study enrolls patients scheduled to undergo curative surgery for colorectal cancer. Bowel sounds will be assessed preoperatively and postoperatively. By comparing intraoperative variables, the incidence of perioperative complications, reoperation rates, and postoperative outcomes-including time to first flatus, resumption of oral intake, and occurrence of intestinal obstruction-this study aims to investigate the association between perioperative bowel sounds and postoperative recovery, and provide evidence-based support for the clinical application of bowel sound monitoring.
Supplementary Definitions
Who can participate
Age range
18 Years – 90 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Aged 18-80 years.
* Histopathologically confirmed colorectal adenocarcinoma according to the WHO 2022 classification.
* No restriction on prior neoadjuvant or other antitumor therapies, including chemotherapy, radiotherapy, targeted therapy, or immunotherapy.
* Able to understand the study requirements and voluntarily provide written informed consent (patient and/or legally authorized representative).
* Able to communicate effectively with the investigators and willing to comply with all study procedures, including postoperative management and follow-up.
Exclusion Criteria:
* Significant organ dysfunction indicating inability to tolerate surgery or an unacceptably high perioperative risk, including:
* Severe cardiac dysfunction (NYHA Class III or IV).
* Severe hepatic dysfunction (MELD score \>12).
* Severe renal dysfunction (eGFR \<30 mL/min/1.73 m² \[CKD stage 4-5\] or end-stage renal disease requiring dialysis).
* Severe pulmonary dysfunction (resting PaO₂ \<60 mmHg on room air or respiratory failure requiring long-term oxygen therapy or mechanical ventilation).
* Participation in another clinical study within 4 weeks before enrollment or concurrent participation in another interventional clinical study.
* Emergency surgery required because of intestinal obstruction, perforation, or other acute abdominal conditions.
* Severe psychiatric disorders that would interfere with compliance with perioperative management or follow-up.
* Pregnant or breastfe…
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Occurrence of postoperative ileus ( POI) after surgery.
Timeframe: From surgery through postoperative day 30