NCT07705139Recruiting
The Value of Bowel Sounds in Evaluating Postoperative Intestinal Function Recovery in Colorectal Cancer Patients
The Value of Bowel Sounds in Evaluating Postoperative Intestinal Function Recovery in Colorectal Cancer Patients: A Prospective Cohort Study
Source: ClinicalTrials.gov · Last updated 15 Jul 2026
Brief summary (registry, in English)
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
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 172 (estimated)
- First submitted
- 3 Jun 2026
- Start date
- 1 Feb 2026
- Primary completion date
- 15 May 2026
- Lead sponsor
- Zhongnan Hospital
- Diseases
- Colorectal cancer
- NCT number
- NCT07705139
What you commit to
- Study type: Observational
- Planned participants: 172
- From 1 Feb 2026 to the primary completion date, 15 May 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Significant organ dysfunction indicating inability to tolerate surgery or an unacceptably high perioperative risk, including:
- Participation in another clinical study within 4 weeks before enrollment or concurrent participation in another interventional clinical study.
Other illness
- Severe cardiac dysfunction (NYHA Class III or IV).
- Severe pulmonary dysfunction (resting PaO₂ \<60 mmHg on room air or respiratory failure requiring long-term oxygen therapy or mechanical ventilation).
- 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.
Lab values
- Severe renal dysfunction (eGFR \<30 mL/min/1.73 m² \[CKD stage 4-5\] or end-stage renal disease requiring dialysis).
- Any other clinical or laboratory abnormality that, in the opinion of the investigator, would make the participant unsuitable for the study.
Other
- Severe hepatic dysfunction (MELD score \>12).
- Pregnant or breastfeeding women.
Who the study is looking for
- 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.
Age in the registry: 18 years to 90 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Zhongnan Hospital of Wuhan University Coordinator of this site? Confirm its status | Wuhan | China | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.