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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: NCT05245331 Recruiting - Clinical trials for Low Anterior Resection Syndrome

Transanal Irrigation for Low Anterior Resection Syndrome.

HiLoV_TAI
Start date: August 4, 2022
Phase: N/A
Study type: Interventional

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).

NCT ID: NCT05129215 Completed - Rectal Cancer Clinical Trials

Development and Validation of The Post-RT LARS Prediction Model (PORTLARS)

PORTLARS
Start date: March 6, 2020
Phase:
Study type: Observational

Bowel dysfunction is common after a restorative rectal cancer resection. Neoadjuvant radiotherapy is an influential factor that impairs bowel function and quality of life. However, almost half patients who have received primary surgery with preoperative radiotherapy are able to restore a good or moderate bowel function in the long term. This multicenter observational study aims to identify the risk factors of severe bowel dysfunction after rectal cancer resection and neoadjuvant radiotherapy, in accordance with the LARS score, and to build a model that predicts long-term major LARS in the early stage of follow-up. Development and validation cohorts are enrolled from tertiary hospitals in China.

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.

NCT ID: NCT05020132 Completed - Clinical trials for Low Anterior Resection Syndrome

Bowel Dysfunction After Rectal Cancer Treatment

Start date: November 1, 2015
Phase:
Study type: Observational [Patient Registry]

Bowel dysfunction after rectal cancer treatment may significantly affect the quality of life. Our study aimed to estimate the incidence and characterize the Low Anterior Resection Syndrome(LARS). We performed a prospective evaluation of patients treated with anterior resection for rectal cancer at two hospitals. Assessment was performed at baseline, after neoadjuvant treatment, and 1, 6 and 12 months after bowel transit reconstruction using the following scores: Bristol scale, LARS score, MSK-BFI, FIQL, EORTC-QLQ30 and a visual analogue scale.

NCT ID: NCT05016583 Completed - Clinical trials for Low Anterior Resection Syndrome

Paula Method of Exercises in Patients With LARS Syndrome

Start date: October 28, 2021
Phase: N/A
Study type: Interventional

Sphincter sparing rectal resection surgery, either total mesorectal excision (TME) with a temporary loop ileostomy or partial mesorectal excision (PME), is the mainstay of rectal cancer treatment , however, these treatments are associated with the development of Low anterior resection syndrome (LARS). This syndrome is characterized by a constellation of symptoms such as fecal frequency, urgency and clustering of bowel movements and can lead to fecal and flatus incontinence. There is no gold standard therapy designed to treat the root cause of the problems associated with LARS. Paula Method of exercises, based on the theory that the body has the natural ability to self-heal and that all sphincter muscles in the body affect one another other and thus, exercising one healthy region can positively impact another. The purpose of this study is to evaluate the feasibility of the Paula Method of exercises in patients post sphincter sparing rectal resection surgery with LARS Syndrome.

NCT ID: NCT05007015 Recruiting - Rectal Cancer Clinical Trials

Transanal Irrigation for the Management of LARS

TAI-LARS
Start date: January 15, 2022
Phase: N/A
Study type: Interventional

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.

NCT ID: NCT04991688 Terminated - Clinical trials for Refractory Medical Treatment After Rectal Resection

A Prospective Pilot Study to Assess the Efficacy of BOTOX-A in Patients With Low Anterior Resection Syndrome (LARS>20) and Refractory Medical Treatment After Rectal Resection

BOTOX-TME
Start date: September 1, 2021
Phase: Phase 2
Study type: Interventional

After rectal resection for cancer (with or without stoma), patients may have digestive sequelae. LARS (Low Anterior Resection Syndrome) includes bowel frequency, stool fragmentation, urgency, and faecal incontinence. The goal of this study is to test intra-rectal BOTOX-A on functional outcomes and quality of life of patients with LARS refractory to medical treatment at 3 months after surgery.

NCT ID: NCT04966819 Recruiting - Rectal Cancer Clinical Trials

Rectal Cancer Shared Care

Start date: March 1, 2022
Phase: N/A
Study type: Interventional

The investigators propose a multifaceted rectal cancer survivorship care program involving oncology specialists, nursing support and primary care physicians. This initiative centers on regular meetings with oncology nursing support, enhanced communication and coordination of care among clinicians including primary care physicians, and an educational platform for patients regarding the late and long-term effects of cancer. Initial efforts will target rectal cancer patients specifically as they have been identified as being at high risk of having unmet needs. Once we have realized measurable, successful implementation in this population, our hope is then to expand our initiative to all colon cancer patients.

NCT ID: NCT04938336 Recruiting - Rectal Cancer Clinical Trials

Evaluation of a Decision Aid Tool in Rectal Cancer patiënts

Start date: April 22, 2022
Phase:
Study type: Observational

Adapt and evaluate a decision aid for patients with rectal cancer. Phase 1 : decision aid testing (Delphi) multicentric Phase 2: pilot test decision aid

NCT ID: NCT04896879 Completed - Rectal Cancer Clinical Trials

Experiences and Needs of Patients, Their Informal Caregiver and Healthcare Professionals Regarding LARS

Start date: November 22, 2016
Phase:
Study type: Observational

Exploration of the experiences and needs of patients with the low anterior resection syndrome, their informal caregiver and health care professionals. This is a qualitative study where semi-structured interviews will be conducted with patients and informal caregivers. next to that focus groups will be performed with healthcare professionals from different professions.