Long-term evaluation of surgical outcomes for rectal cancer treatment

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This cohort study aims to evaluate and compare the surgical, oncological, and functional outcomes, as well as the quality of life, following total mesorectal excision for rectal cancer. It will analyze data from medical records and assess both retrospective outcomes from 2007-2016 and prospective outcomes from 2017-2026. The study will focus on bowel and urogenital function, along with quality of life metrics, measured at diagnosis and after stoma reversal. Variations in treatment approaches will also be examined for their impact on these outcomes.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Men and Women \>18 years
* Patients with rectal cancer
* Underwent mesorectal excision
* Agreed to fill in a validated questionnaires before surgery and after stoma reversal
* Informed consent

Exclusion Criteria:

* Age \< 18
* No informed consent (no general consent, no consent to use personal data for research purpose)

Where it's running

• Kantonsspital Winterthur
  Winterthur, Canton of Zurich, Switzerland Recruiting

Study contacts

• Principal investigator: Michel Adamina, Prof/MD/MSc — Kantonsspital Winterthur KSW
• Study coordinator: Michel Adamina, Prof/MD/MSc
• Email: michel.adamina@ksw.ch
• Phone: +41522663376

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.