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NCT05985239Completed

Virtual Ileostomy Versus Diverting Ileostomy

Comparing the Safety and Efficacy of Virtual Ileostomy Versus Diverting Ileostomy in Patients Underwent Total Mesorectal Excision for Rectal Cancer: a Propensity-matched Study

Source: ClinicalTrials.gov · Last updated 15 Oct 2024

Brief summary (registry, in English)

This study aimed at comparing the Comprehensive Complication Index (CCI), readmission rates, postoperative hospitalization days, duration of bearing the stoma (months), hospitalization costs, the number of hospitalizations with virtual ileostomy versus conventional divertingileostomy after total mesorectal excision for rectal cancer.

Status (registry)
Completed
Study type
Observational
Enrollment
612 (actual)
First submitted
14 Jul 2023
Start date
1 Jan 2023
Primary completion date
10 Oct 2024
Lead sponsor
fan li
NCT number
NCT05985239

What you commit to

  • Study type: Observational
  • Participants enrolled: 612
  • From 1 Jan 2023 to the primary completion date, 10 Oct 2024
  • 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

  • Emergency surgery, open surgery
  • 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
  • Intraoperative combined multi-organ resection

Other illness

  • Long-term history of using immunosuppressants or glucocorticoids
  • Chronic renal failure (requiring dialysis or glomerular filtration rate \<30 mL/ min)

Other

  • ASA score \>3points
  • Patients with combined complete intestinal obstruction
  • Combined cirrhosis of the liver
  • Intraoperative findings of incomplete anastomosis and positive insufflation test
  • missing information

Who the study is looking for

  • Diagnosis of rectal cancer confirmed by pathology
  • Age ≥ 18 years
  • Lap/robot 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)
  • Ability to understand the nature and risks of participating in the trial

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Daping Hospital, Third Military Medical University
Coordinator of this site? Confirm its status
ChongqingChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.