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Clinical Trial Summary

Intra-hospital transport is a frequent procedure in the ICU, involving patients with the highest severity scores. Although some studies estimate the rate of adverse events to be around 33% during intra-hospital transport, including 4% of serious adverse events, the epidemiological data available is small, heterogeneous, and probably subject to methodological bias. The aim of this study observational prospective observatoinal study is to determine: - the different practices existing between ICUs ("practice survey") - the occurrence of adverse events during intra-hospital transport provided by intensive care units (epidemiological study)


Clinical Trial Description

This is a multicenter prospective observational study on evaluation of practices between ICUs and to describe the occurence of adverse events during intra-hospital transport provided by ICUs (epidemiological study) ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06455696
Study type Observational
Source French Society for Intensive Care
Contact Raphaël CLERE-JEHL
Phone +33 1 45 86 51 99
Email raphael.clere@gmail.com
Status Recruiting
Phase
Start date January 1, 2024
Completion date June 30, 2025

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