Skip to content
TrialMatch
Sign up
Recruiting

Virtual Ileostomy Versus Diverting Ileostomy in Patients Undergoing Total Mesorectal Excision

Create a profile to match View the full record on ClinicalTrials.gov

About this study

The goal of this clinical trial is to learn to compare the safety and efficacy of virtual ileostomy versus diverting ileostomy in patients undergoing sphincter-saving surgery for rectal cancer. The main questions it aims to answer are: * Is the virtual ileostomy a safe and effective alternative to the ileostomy? * Is it scientifically reasonable to perform diverting ileostomy intraoperatively? Researchers will compare virtual ileostomy to diverting ileostomy to see if the virtual ileostomy works to reduce rates of stoma. Participants will: * Performing diverting ileostomy or virtual ileostomy undergoing sphincter-saving surgery for rectal cancer * Continuous follow-up of their complications after the first surgery

Condition
Rectal Cancer
Tested
Virtual ileostomy
Sponsor
Daping Hospital and the Research Institute of Surgery of the Third Military Medical University

Who can join

Age
18 years and older
Sex
All sexes
Healthy volunteers
Not accepted

Inclusion 7

  • Minimum age: 18 years
  • Study condition: Rectal Cancer
  • Diagnosis of rectal cancer confirmed by pathology
  • Age ≥ 18 years
  • Total mesorectal excision (TME) surgical procedures and colon-rectum or colon-anal anastomosis：1.anterior resection (AR/ PME), 2. low anterior resection (LAR) , 3.intersphincteric abdominoperineal resection (ISR), 4.transanal total mesorectal excision (TaTME)
  • Signed informed consent
  • Ability to understand the nature and risks of participating in the trial

Exclusion 12

  • Emergency surgery, open surgery
  • ASA score \>3points
  • Patients with combined complete intestinal obstruction
  • Long-term history of using immunosuppressants or glucocorticoids
  • Combined severe cardiac disease: with congestive heart failure or NYHA cardiac function ≥ grade 2. Patients with a history of myocardial infarction or coronary artery surgery within 6 months before the procedure
  • Chronic renal failure (requiring dialysis or glomerular filtration rate \<30 mL/min)
  • Intraoperative combined multi-organ resection
  • Combined cirrhosis of the liver
  • Intraoperative findings of incomplete anastomosis and positive insufflation test
  • Modified Bacon procedure(Two-Stage Turnbull-Cutait Pull-Through Coloanal Anastomosis)
  • Due to an intraoperative accident the surgeon felt that a diverting ileostomy was necessary.
  • Currently participating in other clinical trials

Where

1 site, 1 recruiting

Daping Hospital, Third Military Medical University

Chongqing, China

Recruiting

Contact

Potential match only. Final eligibility is determined by the study team.