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NCT05623176 Clinical Trial

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

Abdomen, Acute Clinical Trial

— LAPTOP  

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?

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05623176
Other study ID # K2022-9097
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 2015
Est. completion date December 2021

Study information
Verified date October 2023
Source Region Stockholm
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The goal of this retrospective observational cohort study is to evaluate the current standard of care for general surgerical patients undergoing emergency laparotomy and assess factors affecting clinical outcomes. 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 This is a mapping of current standards of care prior to the implementation of a standardised care protocols for emergency laparotomy patients.

Recruitment information / eligibility
Status Completed
Enrollment 1000
Est. completion date December 2021
Est. primary completion date December 2020
Accepts healthy volunteers No
Gender All
Age group 16 Years and older
Eligibility Inclusion Criteria: - Undergoing emergency laparotomy due to general surgical indication Exclusion Criteria: - Children under 16 - Trauma laparotomy - Vascular or gynaecological indication for laparotomy

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Region Stockholm

Outcome
Type Measure Description Time frame Safety issue
Primary In-hospital mortality 30 days
Secondary In-hospital serious complications 30 days
Secondary Long-term mortality One year
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