Actively Recruiting
Improvement in Patient Survival and Equality in Care Provision for General Surgery Patients Undergoing Emergency Laparotomy Through Standardised Care Protocols
Led by Region Stockholm · Updated on 2024-12-11
2000
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to evaluate the current standard care for general surgical patients undergoing emergency laparotomy, focusing on factors that affect clinical outcomes and the quality of life in the year following abdominal surgery. It seeks to understand what factors are linked to adverse post-operative events, whether care differs based on sex or age, and how quality of life changes over time. The study also plans to compare outcomes before and after introducing standardized care protocols for these patients. The study observes two groups: one receiving the traditional care routine without standardized protocols and another treated under a newly introduced standardized laparotomy care protocol. No experimental treatments are given as part of the study; rather, the study compares outcomes between these two existing care approaches. This approach allows the assessment of improvements in patient survival and equality in care provision. Participants will be monitored for outcomes including in-hospital mortality within 30 days, serious complications during the hospital stay within 30 days, long-term mortality over one year, and responses to quality of life questionnaires during the year after surgery. Data collection and evaluation will help assess the effectiveness and equality of care over time. The overall participation duration spans one year after the surgery procedure.
CONDITIONS
Brief Title
Clinical Outcomes and Equality in Healthcare for Emergency General Surgery Patients Undergoing Emergency Laparotomy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Undergoing emergency laparotomy due to general surgical indication
You will not qualify if you...
- Children under 16 years old
- Laparotomy due to trauma
- Laparotomy due to vascular, urological, or gynecological indications
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to hospital discharge or 30 days
Participants undergo emergency laparotomy under either the old routine or new standardised care protocols as part of routine clinical care.
Hospital stay with routine clinical assessments
Duration - Up to 1 year
Participants are followed for outcomes including serious complications, mortality, and quality of life assessments.
Follow-up visits or remote assessments up to 1 year
Trial Site Locations
Total: 1 location
1
Karolinska University Hospital
Stockholm, Sweden, 17176
Actively Recruiting
Research Team
R
Rebecka Ahl Hulme, MD PhD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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