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NCT07132970Recruiting

Leakage Rate of Ileo-COlic Sutured Anastomosis After Right Hemicolectomy

Assessment of the Leakage Rate of Ileo-colic Sutured Anastomoses Using a Polydioxanone Based Suture Material After Laparoscopic or Open Right Hemicolectomy to Treat Malignancy

Source: ClinicalTrials.gov · Last updated 9 Jun 2026

Brief summary (registry, in English)

The primary aim of the study is to show that the ileo-colic anastomosis leakage rate until the first 30 days after surgery using MonoPlus® suture material for anastomosis construction after right hemicolectomy is not inferior to the anastomosis leakage rate published in the literature for totally handsewn or stapled-handsewn ileo-colic anastomosis.

Status (registry)
Recruiting
Study type
Observational
Enrollment
249 (estimated)
First submitted
2 Jul 2025
Start date
26 Jan 2026
Primary completion date
Jul 2027
Lead sponsor
Aesculap AG
NCT number
NCT07132970

What you commit to

  • Study type: Observational
  • Planned participants: 249
  • From 26 Jan 2026 to the primary completion date, Jul 2027
  • 4 sites 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

  • Left hemicolectomy or left extended hemicolectomy or sigma resection
  • Emergency surgery
  • Previous abdominal surgery with bowel resection
  • Re-operation of an anastomosis (anastomosis revision surgery)

Other illness

  • Inflammatory bowel disease (e.g. Crohn´s disease)

Other

  • Need for stoma creation
  • Non-compliant patients
  • Participation in an interventional randomized controlled study (RCT)

Who the study is looking for

  • Patients undergoing a primary, elective either open or laparoscopic right hemicolectomy or right extended hemicolectomy due to malignancy with the creation of an intracorporeal or extracorporeal ileo-colic anastomosis.
  • Either complete hand-sewn anastomosis or partial sutured anastomosis (e.g. combination of stapling and suturing)
  • Open or laparoscopic as well as conversion from open to laparoscopic surgery
  • Absence of peritoneal carcinomatosis
  • Absence of vascular, nervous or bone infiltration
  • Age ≥ 18 years
  • Written data protection declaration (Written Informed consent)

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

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

SiteCityCountrySite status
AGAPLESION ELISABETHENSTIFT, Klinik für Allgemein- und Viszeralchirurgie
Coordinator of this site? Confirm its status
DarmstadtGermanyRecruiting
Alb-Fils-Klinikum Göppingen, Dept. General Surgery
Coordinator of this site? Confirm its status
GöppingenGermanyRecruiting
Städtisches Klinikum Lüneburg, Dept. General Surgery
Coordinator of this site? Confirm its status
LüneburgGermanyRecruiting
Diakonie-Klinikum Landkreis Schwäbisch Hall, Dept. General Surgery
Coordinator of this site? Confirm its status
Schwäbisch HallGermanyRecruiting

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