Pre-emptive Endoscopic Vacuum Therapy Reduces the Incidence of Anastomotic Leakage After Colorectal Cancer Surgery
Recruiting · NCT07208786 · Interventional (participants receive a specific treatment) · Lead sponsor: Nanchong Central Hospital
View the official record on ClinicalTrials.gov →Interventions studied
What this trial is about
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.
Who can take part
Inclusion criteria
- 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.
Exclusion criteria
- 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.
- History of abdominal radiotherapy or multiple abdominal surgeries leading to severe intra-abdominal adhesions.
- Complicated by other malignant tumors and currently undergoing radiotherapy or chemotherapy.
- Psychiatric illness or cognitive impairment preventing compliance with the study.
Where it is running
1 location listed.
- Nanchong Central Hospital - Nanchong, Sichuan, China