Evaluating outcomes and care equality for patients undergoing emergency laparotomy
Official title: Improvement in Patient Survival and Equality in Care Provision for General Surgery Patients Undergoing Emergency Laparotomy - Can This be Achieved Through the Implementation of Standardised Care Protocols?
Run by Region Stockholm · NCT05623176 · Data updated 2026-11-12
This study looks at how well patients do after emergency surgery for their stomach and what factors, like age and gender, might affect their recovery and quality of life.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 16 Years and up |
| Sex | All |
| Enrollment | 2000 (estimated) |
| Sponsor | Region Stockholm Government |
| Locations | 1 site (Stockholm) |
| Status | Recruiting |
| Started | January 1, 2015 |
| Main results expected | December 2030 |
| Study ends | December 2030 |
| Registry record updated | December 11, 2024 |
| Trial ID | NCT05623176 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are adults undergoing emergency laparotomy for general surgical indications.
✕Probably not a fit
Patients under 16 years old or those undergoing laparotomy for trauma, vascular, urological, or gynecological reasons may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational cohort study aims to assess the standard of care for patients undergoing emergency laparotomy, focusing on factors that influence clinical outcomes and quality of life in the year following surgery. It seeks to identify associations between adverse post-operative events and variables such as age and sex. Additionally, the study will evaluate the current practices before implementing standardized care protocols and will compare outcomes over time. The findings will provide insights into the effectiveness of care and potential disparities in treatment.
Why it matters
Potential benefit: If successful, this study could lead to improved clinical outcomes and quality of life for patients undergoing emergency laparotomy.
How similar studies have gone: Other studies have shown success in evaluating surgical outcomes and care protocols, indicating that this approach is supported by existing research.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Undergoing emergency laparotomy due to general surgical indication Exclusion Criteria: * Children under 16 * Trauma laparotomy * Vascular, urological or gynaecological indication for laparotomy
Where it's running
-
Karolinska University Hospital
Stockholm, Sweden Recruiting
Study contacts
- Principal investigator: Rebecka Ahl Hulme, MD PhD — Karolinska University Hospital
- Study coordinator: Rebecka Ahl Hulme, MD PhD
- Email: rebecka.ahl-hulme@regionstockholm.se
- Phone: 0046812373212
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.