New online training could ease bowel troubles after rectal cancer
NCT ID NCT05007015
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether transanal irrigation (using water to flush the bowel) can improve quality of life and reduce bowel symptoms in 66 rectal cancer survivors who have low anterior resection syndrome (LARS). Participants learn the technique through an online platform with virtual nursing support. The goal is to see if this approach is practical and helpful for Canadian patients.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 66 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2022
- Expected to finish
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Jun 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Low anterior resection by a laparoscopic, robotic, transanal total mesorectal excision, or open approach with (or without) creation of a diverting loop ileostomy for the treatment of rectal cancer, advanced adenoma or dysplasia And * have had their ileostomy closed (if applicable) And * completed treatment at least 6 months ago (including ileostomy closure) And * LARS score \> 20 points Exclusion Criteria: * Inability to provide informed consent, including insufficient fluency in English or French. * Inability to access the internet. * Presence of an ostomy at the time of study enrollment. * Active or ongoing treatment for rectal disease. * Anastomotic stricture, sinus, or any other ongoing anastomotic complication. * Current use of TAI under the direction of a clinical team.
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Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Centre de Recherche du CHU de Québec - Hôpital Saint-François d'Assise
Québec, Quebec, G1L 3L5, Canada
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Health Science North
Greater Sudbury, Ontario, P3E 5J1, Canada
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Jewish General Hospital
Montreal, Quebec, H3T 1E2, Canada
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London Health Science Centre
London, Ontario, N6A 5W9, Canada
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McGill University Health Centre
Montreal, Quebec, Canada
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Providence Hospital - St. Paul's Hospital
Vancouver, British Columbia, V6Z 1Y6, Canada
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University Health Network
Toronto, Ontario, M5G 2C4, Canada
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University of British Columbia - Island Health Colorectal Surgery
Victoria, British Columbia, V8R 6R5, Canada
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Other studies related to the condition(s) this trial covers.
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