Clinical Trial

Transanal Irrigation for the Management of LARS

Study acronym: TAI-LARS
Active, Not Recruiting
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Record status
This record was last updated June 2, 2026 (before its estimated June 30, 2026 completion). Its status may not reflect the trial's current state.
Summary
This study aims to evaluate the impact of Transanal irrigation (TAI) on the quality of life and low anterior resection symptoms (LARS) in Canadian rectal cancer survivors living with minor to major LARS. It proposes to teach TAI through a novel online platform and to provide virtual nursing support for the participants. To our knowledge, this is the first North American based and largest randomized control trial on the use of TAI for patients with LARS. This will also be the first study to teach and support patients through the TAI process using a virtual platform. While TAI has been demonstrated to reduce LARS scores and increased QoL in patients with significant LARS, its feasibility and acceptance for Canadian patients remains uncertain. Furthermore despite the existing studies, the rate of TAI seems to be low in North America. The hypothesis is that TAI, taught and supported through an online portal dedicated to LARS patients, will positively impact QoL and improve LARS symptoms. The results of this trial may allow TAI to become part of the standard armamentarium that clinicians offer patients for LARS management, with the presence of online nursing support and guidance to facilitate this practice.
Protocol Amendment History 5 amendments
This ClinicalTrials.gov record has been amended 5 times since 2021-08-10; most recent amendment 2026-05-29.
Status change: Recruiting → Active, Not Recruiting 2025-07-25
Status change: Not Yet Recruiting → Recruiting 2022-01-18
Trial Details
NCT Number NCT05007015
Lead Sponsor Jewish General Hospital
Collaborators: McGill University Health Centre/Research Institute of the McGill University Health Centre
Conditions Low Anterior Resection Syndrome, Rectal Cancer
Enrollment 66 participants
Start Date 2022-01-15
Primary Completion 2026-06-30 (estimated)
Study Completion 2026-06-30 (estimated)
Updated on ClinicalTrials.gov 2026-06-02