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Low Anterior Resection Syndrome clinical trials

View clinical trials related to Low Anterior Resection Syndrome.

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NCT ID: NCT05445245 Active, not recruiting - Rectal Cancer Clinical Trials

The Longitudinal Study of Low Anterior Resection Syndrome in Patients With Newly Diagnosed Rectal Cancer.

Start date: April 14, 2022
Phase:
Study type: Observational

The aims are to identify the trajectory of LAR Syndrome and explore the adaptation process and coping strategies of LAR Syndrome in patients newly diagnosed with rectal cancer. The participants will recruit from a CRC surgical outpatient department of a medical center in northern Taiwan.

NCT ID: NCT05319054 Active, not recruiting - Clinical trials for Low Anterior Resection Syndrome

Pathway of Low Anterior Resection Syndrome Relief After Surgery: a Feasibility Study

POLARiS
Start date: May 23, 2022
Phase: N/A
Study type: Interventional

Currently, no standard exists for the treatment and management of Low Anterior Resection Syndrome (LARS)- a common disorder that affects patients who have had part of their bowel removed due to colorectal cancer. Decisions about which treatment patients receive is at the discretion of local clinicians, leading to a variation in both clinical practice and the outcomes of these patients. As a result, there is a need for research to assess what treatments are most effective in treating or managing LARS to establish a consensus and develop a treatment pathway in the UK. This study aims to assess the feasibility of undertaking such a trial utilising a novel 'trial within cohorts (TWiCs)' study design, with a view to informing the design of a full-scale trial.

NCT ID: NCT05042700 Active, not recruiting - Clinical trials for Low Anterior Resection Syndrome

The Effect of Melatonin in Patients With Low Anterior Resection Syndrome

MELLARS
Start date: October 13, 2021
Phase: Phase 2
Study type: Interventional

The primary objective of the study is to investigate whether treatment with melatonin has an alleviating effect on Low Anterior Resection Syndrome (LARS) symptoms. Secondarily, the effect of the treatment on bowel movements, other patient reported symptoms, quality of life, depression, anxiety, sleep disturbances, motilin levels, and microscopic changes in rectal mucosa will be investigated.