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Stoma Function and Quality of Life After Emergency or Planned Surgery in Colorectal Cancer

Compares daily life and wellbeing in colorectal cancer patients with emergency or planned stomas.

Plain-language title generated from the registry record
Registry title: Function and Quality of Life After Emergency vs Planned Creation of a Stoma

Key facts

Where
Gothenburg, SwedenSee the site

Where in Sweden

  • Gothenburg University, Sahlgrenska Academy, Institute of Cinical Sciences, Department of SurgeryGothenburg, SwedenNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Eva Haglind, MD, PhD, professor
Trial code
NCT05102981
Record updated
27 April 2026
Original description
The aim is to compare functional outcome and or quality of life in patients with a stoma that was constructed as an emergency procedure with patients where a stoma was created as a planned procedure. To do this data will be retrieved from the Swedish Patient Register to identify all patients with a diagnosis of colorectal cancer and a stoma construction procedure during two previous calender years. To collect data on stoma function and quality of life a specific questionnaire will be sent to the cohort approximately within 2 years of the procedure.Read full original descriptionShow less

StomaFUNQ. Function and Quality of Life After Emergency vs Planned Creation of a Stoma

The aim is to compare functional outcome and or quality of life in patients with a stoma that was constructed as an emergency procedure with patients where a stoma was created as a planned procedure. To do this data will be retrieved from the Swedish Patient Register to identify all patients with a diagnosis of colorectal cancer and a stoma construction procedure during two previous calender years. To collect data on stoma function and quality of life a specific questionnaire will be sent to the cohort approximately within 2 years of the procedure.

Inclusion: stoma permanently or for shorter period.

Exclusion: not understanding Swedish.

ClinicalTrials.gov NCT05102981