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
• Status: Recruiting
• 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
• 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

Related Conditions & MeSH terms

• Emergencies
• Emergency Surgery
• Mortality

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