Skåne University Hospital
Malmö, Sweden
Location status: Recruiting
NCT Number: NCT06214988
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.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Malmö, Sweden
Location status: Recruiting
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Additional inclusion criteria for randomised part of the study:
Exclusion criteria
->2 staple firings for rectal transection
With randomisation to this experimental arm (selective approach), no defunctioning stoma is constructed.
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.
Time frame: 1,3,12 and 24 months
ISREC grading
Time frame: 1,3,12 and 24 months
Clavien-Dinco
Time frame: until discharge within 90 days
total days in hospital
Time frame: 3 months
death
Time frame: 12 and 24 months
domain score scale 0-42 points, >30 points indicate a bad functional outcome i.e. major LARS
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.
Time frame: 1 month
Difference from baseline in total score 0-150 points, higher value indicating faster recovery
Time frame: 12 months
Clinical assessment categorisation
Time frame: 12 and 24 months
Creatinine (mg/L)
Time frame: 24 months
total days of alive and out of hospital
Time frame: 24 months
proportion
Time frame: 36 and 60 months
Clinical assessment categorisation
Time frame: 36 and 60 months
Clinical assessment categorisation
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.
Contact information is provided by the study sponsor or research team.
Skane University Hospital
Other
SELective Defunctioning Stoma Approach in Low Anterior Resection for Rectal Cancer (SELSA): a Prospective Study With a Nested Randomised Clinical Trial
Acronym: SELSA
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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.
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