140
Participants
Start Date
August 1, 2025
Primary Completion Date
May 1, 2028
Study Completion Date
July 1, 2028
Intensified follow-up program
The study intervention will be an intensified follow-up program which consists of different measures. Patients will attend follow-up visits 1, 4, 7 and 13 months after ileostomy repositioning, at which LARS symptoms, quality of life as well as sexual and urinary function will be recorded using various questionnaires. In case of LARS symptoms patients will receive medical treatment with loperamide and metamucil as well as pelvic floor muscle training (including biofeedback and home exercises). Regarding pelvic floor muscle training we are planning nine sessions instructed by physiotherapy staff. In case of therapy-resistant LARS symptoms after 6 months sacral neurostimulation is offered to the patients with a focus on incontinence symptoms and desire for surgery or transanal irrigation in patients with a focus on voiding disorders. In case of urinary and sexual complaints patients are referred to our urology or gynaecology department for further diagnostic and treatment.
Clarunis Universitäres Bauchzentrum Basel, Basel
Lindenhofspital Bern, Bern
St. Anna Spital Bern, Bern
Kantonsspital Luzern, Lucerne
Kantonsspital Winterthur, Winterthur
St. Claraspital AG
OTHER
Clarunis - Universitäres Bauchzentrum Basel
OTHER
University Hospital, Basel, Switzerland
OTHER