Ireland
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Recruiting Observational

Clinical Outcomes and Equality in Healthcare for Emergency General Surgery Patients Undergoing Emergency Laparotomy

NCT05623176 · tracked via the Priya Life Science Sweden tracker
Phase
Observational
Started
2015-01-01
Last updated
2024-12-11

Condition(s) studied

Abdomen, Acute

Investigational drug(s) / intervention(s)

Standardised laparotomy care

Standardised laparotomy care: This is a cohort study and no intervention as part of the study has been introduced. We are studying two groups and comparing the two before and after the introduction of a standardised laparotomy care protocol as part of a clinical quality improvement measure.

Study summary

The goal of this observational cohort study is to evaluate the standard of care for general surgerical patients undergoing emergency laparotomy and assess factors affecting clinical outcomes, as well as evaluating the quality of life in the year after abdominal surgery.

The main questions it aims to answer are:

1. what factors are associated with adverse post-operative events
2. are patients treated differently based on sex or age
3. how does quality of life look like and possibly change over the coarse of a year after surgery

This is an evaluation of the current standard of care and the outcomes of this patient group prior to the implementation of a standardised care protocols for emergency laparotomy patients. Secondly, the study aims to, over time, compare results before and after the introduction of this standardised care protocol.

Eligibility

Sex
ALL
Min age
16 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Undergoing emergency laparotomy due to general surgical indication Exclusion Criteria: * Children under 16 * Trauma laparotomy * Vascular, urological or gynaecological indication for laparotomy

Primary outcome measure(s)

  • In-hospital mortality — 30 days

Trial sites (1)

FacilityCityRegionStatus
Karolinska University Hospital Stockholm Sweden Recruiting
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 NCT05623176 on ClinicalTrials.gov ↗ ← All trials in Sweden