Clinical Trials Logo

Clinical Trial Summary

Multicenter retrospective study conducted in the intensive care units of Tourcoing, Roubaix, and Lille hospitals. Patients hospitalized in the ICU with EBLSE bacteremia within 24 hours before or during their stay in the ICU will be selected from microbiology laboratory data. Patient demographics and clinical data will be collected from the medical record. Microbiological results will be collected from the laboratory data.


Clinical Trial Description

INCLUSION CRITERIA - Patients admitted to the ICU with EBLSE bacteremia within 24 hours before or during their stay in the ICU. PRIMARY ENDPOINT - The primary endpoint is 30-day mortality. ;


Study Design


NCT number NCT05833282
Study type Observational
Source Tourcoing Hospital
Contact MEYBECK Angès, MD
Phone 0320694238
Email recherche@ch-tourcoing.fr
Status Recruiting
Phase
Start date July 1, 2022
Completion date June 30, 2023