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NCT05888948 Clinical Trial

Surgical Emergencies Gradation and Postoperative Outcome

Mortality Clinical Trial

— BUGRADA  

Official title:
Effect of Implementation of a Surgical Emergencies Gradation on Postoperative Outcome in Emergency Operating Theatre Patients of the Amiens-Picardy University Hospital

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05888948
Other study ID # PI2022_843_0056
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 25, 2022
Est. completion date April 2024

Study information
Verified date May 2023
Source Centre Hospitalier Universitaire, Amiens
Contact Stéphane BAR, MD
Phone 03 22 08 79 06
Email bar.stephane@chu-amiens.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Reducing surgical waiting time has been shown to be associated with a reduction in postoperative morbidity and mortality in this type of surgery. The use of a gradation of surgical emergencies makes it possible to prioritise them in an objective, consensual manner and to carry them out within a theoretical expected waiting time relative to the degree of urgency. The investigators hypothesise that exceeding the theoretical expected waiting time relative to the degree of urgency defined by the gradation of surgical emergencies is associated with an increase in postoperative morbidity and mortality in emergency surgery. The objective is to assess the impact on post-operative morbidity and mortality of waiting times exceeding the theoretical expected time by grading the surgical emergencies of patients undergoing emergency surgery.

Recruitment information / eligibility
Status Recruiting
Enrollment 700
Est. completion date April 2024
Est. primary completion date April 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - age > 18 years old. - Non-cardiac emergency surgery. Exclusion Criteria: - Minor patients - Emergency cardiac surgery - Patients under guardianship or curators - Pregnant women - Patients who object to their personal data being used in research

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
France CHU Amiens-Picardie Amiens

Sponsors (1)
Lead Sponsor Collaborator
Centre Hospitalier Universitaire, Amiens

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Number Post-operative complications 1 year
Primary Mortality at 1 year 1 year
Primary Length of stay in intensive care unit 1 year
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