About this trial
Evaluate the safety and efficacy of postoperative Pre-emptive EVT (PEVT) in reducing the incidence of anastomotic leaks within 30 days after surgery in patients with colorectal cancer. Compare the differences between the PEVT group and the control group in terms of operation time, length of hospital stay, and total medical costs. Analyze the incidence of other postoperative complications in the two groups, such as wound infection, abdominal abscess, and intestinal obstruction. Assess the impact of PEVT on postoperative recovery indicators, including time to first flatus, time to first defecation, and time to ambulation. Observe the occurrence of PEVT-related adverse events, such as device displacement, bleeding, and infection.
Eligibility criteria
Qualifiers
Pathologically diagnosed with colorectal cancer, planned for radical surgery (right hemicolectomy, left hemicolectomy, or anterior resection of the rectum, etc.).
Age 18-85 years, American Society of Anesthesiologists (ASA) classification I-III.
Anastomosis to be performed in a single stage (meeting anastomotic criteria).
Patient or legal guardian is able to understand and sign the informed consent form and comply with follow-up.
Disqualifiers
Preexisting anastomotic leakage or severe intra-abdominal infection before surgery.
Complicated by severe cardiovascular or cerebrovascular diseases (e.g., acute myocardial infarction, acute phase of cerebral infarction).
Severe liver or kidney dysfunction (liver function Child-Pugh class C, creatinine clearance <30 ml/min).
Coagulation disorders (platelets <50×10⁹/L, INR >1.5) or receiving anticoagulant therapy that cannot be adjusted.
Trial design
Treatments tested in this trial
- PEVT