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Clinical Trial Summary

The goal of this observational study is to examine the clinical presentations, the diagnostic tests performed and the management of patients presenting with transient loss of consciousness (TLOC) The main questions it aims to answer are: - prevalence of TLOC - prevalence of different diagnoses leading to TLOC Demographic, clinical, paraclinical and biological data will be collected from the emergency medical file


Clinical Trial Description

Patients over the age of 18 presenting to the University Hospital of Clermont-Ferrand emergency department for transient loss of consciousness of syncopal or undifferentiated origin will be include. Their non-opposition will be sought. Demographic, clinical, paraclinical and biological data will be collected from the emergency medical file. No visit is planned after the passage to the emergency room. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05575934
Study type Observational
Source University Hospital, Clermont-Ferrand
Contact Lise Laclautre
Phone 334.73.754.963
Email promo_interne_drci@chu-clermontferrand.fr
Status Recruiting
Phase
Start date October 3, 2022
Completion date September 30, 2023

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