Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorBordeaux Colorectal Institute
About this trial
The objectiive of this prospective, international cohort is to compare two anastomotic techniques (DS vs TTSS) by collecting data during the surgery, and postoperatively (morbidity and functional outcomes).
The choice of technique is left to the discretion of the surgeon based on her/his practices.
Eligibility criteria
Qualifiers
Age ≥ 18
Patients with rectal cancer lower than 12 cm from the anal verge requiring either a stapling anastomosis below 7 cm from the anal verge,
Patients with powered mechanical anastomosis (INTOCARE devices)
Patients with no metastasis
Disqualifiers
Patients with handsewn anastomosis
Patients with perforated rectal cancer or preoperative pelvic sepsis ;
Patients with inflammatory bowel disease;
Patients operated on in emergency ;
Trial design
Treatments tested in this trial
- Not listed
Trial groups
400 Participants
are grouped into 1 trial groupSponsors and collaborators
Source ClinicalTrials.gov