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Clinical Trial Summary

The aim of this study is to investigate whether the high-volume transanal irrigation (TAI) performed by the Peristeen Plus® system is superior to the low-volume TAI performed by standard 250ml water enema for the treatment of Low Anterior Resection Syndrome (LARS).


Clinical Trial Description

Most of the patients operated on for rectal cancer present defecatory disfunction symptoms known as Low Anterior Resection Syndrome (LARS) of different degree and severity. Although, transanal irrigation (TAI) has been shown to be useful in improve LARS and quality of life of these patients no evidence exists about the best way to realize TAI in terms of irrigation volume and systems and frequency of irrigation. This crossover randomized controlled trial aims to evaluate the impact of two different type of TAI (high-volume by Peristeen Plus® and low-volume performed by 250ml water enema) on LARS and quality of life in patients with major LARS secondary to low anterior rectal resection (LAR) for primary rectal cancer. The primary outcome is the reduction of LARS score after two months of treatment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05245331
Study type Interventional
Source Hospital Universitari de Bellvitge
Contact Loris Trenti, PhD
Phone +34 932607500
Email loris.trenti@bellvitgehospital.cat
Status Recruiting
Phase N/A
Start date August 4, 2022
Completion date July 1, 2025

See also
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Completed NCT01589471 - The Value of Botox-A for Management of Low Anterior Resection Syndrome Phase 2
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Recruiting NCT05682157 - Paula Method of Exercises in Patients With LARS Syndrome:Randomized Controlled Trial N/A