Understanding and Tailored Treatment of Low Anterior Resection Syndrome
Recruiting
Observational Study
Low Anterior Resection Syndrome
Faecal Incontinence With Faecal Urgency
Faecal Incontinence
Colorectal (Colon or Rectal) Cancer Survivors
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Observational
- Participants needed
- 145 (estimated)
- Sponsor
- Aalborg University Hospital · Other
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About This Trial
The goal of this observational study is to learn why some patients develop low anterior resection syndrome (LARS) after colorectal cancer treatment. The study also aims to identify different subtypes of LARS and understand which patients may respond to specific treatments.
The main questions it aims to answer are:
* What physiological and imaging changes are associated with LARS?
* How do patien…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
General:
* Must be able to read and understand Danish.
* All participants must be adults and \>18 years and have full legal capacity.
* Assessed by study personnel to have understood the research protocol, being able to comply with investigation procedures as well as ability to…
Contacts