Evaluating outcomes and care equality for patients undergoing emergency laparotomy
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?
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 |
|---|---|
| Enrollment | 2000 (estimated) |
| Ages | 16 Years and up |
| Sex | All |
| Sponsor | Region Stockholm Government |
| Locations | 1 site (Stockholm) |
| Trial ID | NCT05623176 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates for this study are adults undergoing emergency laparotomy for general surgical indications.
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.
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 performed: Other studies have shown success in evaluating surgical outcomes and care protocols, indicating that this approach is supported by existing research.
Eligibility criteria
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 this trial is running
Stockholm
- 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
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.