Skip to main content
OpenTrials
Recruiting

NCT Number: NCT06214988

Selective Defunctioning Stoma in Low Anterior Resection for Rectal Cancer

The goal of this observational trial with a nested randomized controlled trial is to investigate a selective approach of defunctioning stoma in low anterior resection in rectal cancer patients. The primary outcome is a hybrid so-called textbook outcome; stoma-free survival at two years without major LARS, reflecting a functionally appropriate outcome after low anterior resection for rectal cancer. Secondary outcomes include anastomotic leakage, postoperative mortality, reinterventions, stoma-related complications, quality of life measures, LARS, and permanent stoma rate up to two years after index surgery.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Skåne University Hospital

Malmö, Sweden

Location status: Recruiting

Location contact

Pamela Buchwald, MD PhD

CONTACT

[email protected]

About this study

Systematic use of defunctioning stoma after low anterior resection for rectal cancer has been shown to reduce symptomatic anastomotic leakage and associated interventions. However, accumulating data suggest that this comes at the price of worse bowel dysfunction, a higher rate of permanent stomas and kidney injury. We aim to study whether a selective strategy of defunctioning stoma use might lead to fewer adverse consequences, while still being safe for patients.

This is a multicentre international prospective trial including a non-blinded randomised clinical trial. All patients with a primary rectal cancer planned for low anterior resection with colorectal or coloanal anastomosis are eligible. Patients enter a prospective observational study, in which a randomised clinical trial is nested. Patients eligible for randomisation are aged below 80 years, have an American Society of Anesthesiologists' fitness grade I or II, have no unresected distant disease, and have a predicted lower risk of anastomotic leakage. Patients will be randomised 1:1 to either an experimental arm with no defunctioning stoma or to a control arm with a defunctioning stoma. The randomisation is computer-generated with a concealed sequence and stratified by participating hospital and radiotherapy use. The main outcome is the composite measure of 2-year stoma-free survival without major low anterior resection syndrome (LARS). Secondary outcomes include anastomotic leakage, postoperative mortality, reinterventions, stoma-related complications, quality of life measures, LARS, and permanent stoma rate up to two years after index surgery. To be able to state superiority of any study arm regarding the main outcome, with 90% statistical power and assuming 25% attrition, we aim to enrol 212 patients.

This study has been approved by Ethical Review Authority in Sweden (2023-04347-01) and seeks permission in Norway and Danmark, respectively. The results will be disseminated through patient associations, popular science, the broader medical community, and conventional scientific channels.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult patients with rectal cancer planned for a low anterior resection with anastomosis by TME with any surgical approach

Additional inclusion criteria for randomised part of the study:

  • Patients aged less than 80 years
  • Patients with American Society of Anesthetists' (ASA) fitness grade I or II as determined by the anaesthesiologist or the surgeon
  • Patients without clear radiological signs of distant disease before rectal cancer surgery (previous metastatic surgery is no exclusion criterion)
  • Anastomotic leak risk score of 0-1
  • Willingness to be randomised

Exclusion criteria

  • Insufficient command of Swedish, Norwegian, Danish or English to understand questionnaires or consent
  • Emergency rectal resection (tumour resection due to large bowel obstruction, perforation, etc)
  • Pregnancy or breastfeeding Additional exclusion criteria for randomised part of the study
  • Previous pelvic irradiation (due to e.g. gynaecological or urological cancer)
  • Preoperative tumour perforation or pelvic sepsis
  • Beyond TME surgery and/or concurrent resection of other organ
  • Concurrent corticosteroid treatment (prednisone-equivalent dosage ≥10 mg daily)
  • Planned postoperative chemotherapy
  • Smoking not completely ceased four weeks before surgery
  • Excessive alcohol consumption with social and medical consequences (as judged by the surgeon in charge) Intraoperative exclusion criteria for randomised part of the study

->2 staple firings for rectal transection

  • Intraoperative blood loss ≥250 ml for minimally invasive surgery
  • Intraoperative blood loss ≥500 ml for open or converted surgery
  • More than one intraabdominal anastomosis performed
  • Incomplete doughnuts
  • Air-leak test positive
  • Any significant intraoperative adverse event at the discretion of the operating surgeon (e.g. ureterotomy, bowel or tumour perforation, major medical event - pulmonary embolism, cardiac arrhythmia) (Gawria, 2022)
  • TME with anastomosis ultimately not done

Treatment and study plan

selective approach defunctioning stoma

Procedure

With randomisation to this experimental arm (selective approach), no defunctioning stoma is constructed.

Primary outcomes

  1. textbook outcome; stoma-free survival at two years without major LARS

    Time frame: 2 year

    extant stoma, alive, and a LARS score at 30 or lesn has stabilised as well for those without a stoma in situ.

    no extant stoma, alive, and a LARS score at 30 or less at the time point two years after the anterior resection.

Secondary outcomes

  1. Anastomotic leakage

    Time frame: 1,3,12 and 24 months

    ISREC grading

  2. Complications

    Time frame: 1,3,12 and 24 months

    Clavien-Dinco

  3. Length of hospital stay

    Time frame: until discharge within 90 days

    total days in hospital

  4. Postoperative mortality

    Time frame: 3 months

    death

  5. Major Low Anterior Resection Syndrome

    Time frame: 12 and 24 months

    domain score scale 0-42 points, >30 points indicate a bad functional outcome i.e. major LARS

  6. Quality of life by European Organization for Research and Treatment of Cancer- ColoRectal 29 (EORTC-CR29)

    Time frame: 12 and 24 months

    EORTC-CR29 domain scores in scales 0-100 points, a high score for the global health status /quality of life represents a high quality of life, but a high score for a symptom scale / item represents a high level of symptomatology / problems.

  7. Quality of Recovery-15 Swedish (QoR15swe)

    Time frame: 1 month

    Difference from baseline in total score 0-150 points, higher value indicating faster recovery

  8. Adjuvant chemotherapy for high-risk patients

    Time frame: 12 months

    Clinical assessment categorisation

  9. Renal function

    Time frame: 12 and 24 months

    Creatinine (mg/L)

  10. Stay out of hospital

    Time frame: 24 months

    total days of alive and out of hospital

  11. Stoma in situ

    Time frame: 24 months

    proportion

  12. Recurrence (local and distant)

    Time frame: 36 and 60 months

    Clinical assessment categorisation

  13. Overall survival

    Time frame: 36 and 60 months

    Clinical assessment categorisation

  14. Quality of life by European Organization for Research and Treatment of Cancer- Cancer30 (EORTC-C30)

    Time frame: 12 and 24 months

    EORTC-C30 domain scores in scales 0-100 points, a high score for the global health status /quality of life represents a high quality of life, but a high score for a symptom scale / item represents a high level of symptomatology / problems.

Study contacts

Contact information is provided by the study sponsor or research team.

Caroline Nilsson, RN

CONTACT

[email protected]

004640331000

Sponsors and collaborators

Lead sponsor

Skane University Hospital

Other

Collaborators

  • Copenhagen University Hospital at Herlev
  • Ersta Hospital, Sweden
  • Göteborg University
  • Linkoeping University
  • Lund University
  • Oslo University Hospital
  • Umeå University
  • Örebro University, Sweden

Registry information

Official study title

SELective Defunctioning Stoma Approach in Low Anterior Resection for Rectal Cancer (SELSA): a Prospective Study With a Nested Randomised Clinical Trial

Acronym: SELSA

Important dates

Study start
2024
Primary completion
2027
Study completion
2030
First posted
Jan 22, 2024
Registry last updated
May 21, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.