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NCT07358247Not yet recruiting

Postoperative Outcomes of Single-stapled Anastomosis Combined With Transanal Natural Orifice Specimen Extraction

Postoperative Outcomes of Transanal Transection and Single-stapled Technique Combined With Transanal Natural Orifice Specimen Extraction: a Single-center Retrospective Cohort Study

Source: ClinicalTrials.gov · Last updated 22 Jan 2026

Brief summary (registry, in English)

Natural Orifice Specimen Extraction (NOSE) eliminates the need for additional abdominal incisions in minimally invasive colorectal procedures, potentially reducing the risk of wound complications and postoperative pain. In the context of restorative Total Mesorectal Excision (TME), single-stapling (SS) techniques facilitate NOSE through transanal rectal transection, as opposed to the conventional double-stapling technique. This study aims to explore the potential advantages of NOSE combined with SS anastomosis compared to conventional abdominal extraction in minimally invasive restorative TME.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
190 (estimated)
First submitted
13 Jan 2026
Start date
31 Jan 2026
Primary completion date
31 Mar 2026
Lead sponsor
Istituto Clinico Humanitas
NCT number
NCT07358247

What you commit to

  • Study type: Observational
  • Planned participants: 190
  • From 31 Jan 2026 to the primary completion date, 31 Mar 2026
  • 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

  • Patients who underwent non-restorative procedures (including abdominoperineal resection or Hartmann's procedures).
  • Patients who underwent open surgery.
  • Patients with a concomitant diagnosis of Inflammatory Bowel Disease (IBD).

Other

  • Patients who underwent immediate or delayed coloanal anastomosis.
  • Patients who underwent unplanned conversion from minimally invasive to open approach.

Who the study is looking for

  • Adult patients aged more than 18 years old at the time of surgery
  • Patients with a histological diagnosis of rectal adenocarcinoma
  • Patients who underwent surgery between January 2017 and January 2023
  • Patients with a low rectal tumor meeting the Low Rectal Cancer Development Programme (LOREC) criteria

Age in the registry: 18 years to - · Sex: All · Does not accept 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
IRCCS Humanitas Research Hospital
Coordinator of this site? Confirm its status
RozzanoItalyUnknown status

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