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Clinical Trials in Sweden / NCT05102981
Enrolling by invitation Observational

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

NCT05102981 · tracked via the Priya Life Science Sweden tracker
Sponsor
Eva Haglind, MD, PhD, professor
Phase
Observational
Started
2024-11-01
Last updated
2026-04-27

Condition(s) studied

Colorectal Cancer

Investigational drug(s) / intervention(s)

emergency procedure

emergency procedure: The difference between groups is the timing or type ie emergency as opposed to planned

Study summary

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * stoma permanently or for shorter period Exclusion Criteria: * not understanding Swedish

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Gothenburg University, Sahlgrenska Academy, Institute of Cinical Sciences, Department of Surgery Gothenburg Sweden

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05102981 on ClinicalTrials.gov ↗ ← All trials in Sweden