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Is transanal irrigation the best treatment possibility for low anterior resection syndrome? A multicenter, randomized clinical trial: study protocol.
Klimovskij, Michail; Civilka, Ignas; Aleinikov, Andrej; Aukstikalnis, Tomas; Christensen, Peter; Dulskas, Audrius.
Afiliación
  • Klimovskij M; Department of Colorectal Surgery, East Sussex Healthcare Trust, Hastings, United Kingdom.
  • Civilka I; Faculty of Medicine, Vilnius University, Vilnius, Lithuania.
  • Aleinikov A; Department of Surgical Oncology, National Cancer Institute, Vilnius, Lithuania.
  • Aukstikalnis T; Faculty of Medicine, Vilnius University, Vilnius, Lithuania.
  • Christensen P; Department of Rehabilitation Physical and Sports Medicine, Faculty of Medicine, Institute of Health Sciences, Vilnius University, Vilnius, Lithuania.
  • Dulskas A; Department of Surgery, Aarhus University Hospital, Aarhus, Denmark.
Front Surg ; 11: 1384815, 2024.
Article en En | MEDLINE | ID: mdl-38803549
ABSTRACT

Background:

Up to 50% of patients who undergo rectal resection suffer from various and partly severe functional problems, despite the preservation of the anal sphincter. These complaints are defined as low anterior resection syndrome (LARS). So far, there are no randomized clinical trials regarding the most effective treatment for LARS. Our aim is to evaluate whether transanal irrigation improves bowel function and quality of life in patients following low anterior resection compared to best supportive care.

Methods:

Patients who have undergone low anterior resection will be approached for this study. On patient's visit, complaints regarding the defecation as well as any deterioration in their overall quality of life will be assessed using questionnaires such as the Low Anterior Resection Syndromes score, Wexner score, European Organization for Research and Treatment of Cancer (EORTC) Quality of Life (QOL) CR-29, and Measure Yourself Medical Outcome Profile tool. Few additional target questions will be also asked, such as "Would you recommend the treatment to anybody; did you expect the improvement following the treatment; etc." Questionnaires and scales will be filled on follow-up visits every 3 months for 1 year.

Discussion:

This multicenter, randomized controlled trial will lead to a better understanding of LARS treatment. Moreover, it will be a hypothesis-generating study and will inform areas needing future prospective studies. Clinical Trial Registration ClinicalTrials.gov, identifier (NCT05920681).
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Surg Año: 2024 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Surg Año: 2024 Tipo del documento: Article País de afiliación: Reino Unido
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