Creation of a Syncope Channel for Patients Admitted to the Emergency Department for Loss of Consciousness and Not Hospitalized: Etiological Predictivity (Before/After Study)

NAActive, not recruitingINTERVENTIONAL
Enrollment

52

Participants

Timeline

Start Date

March 31, 2024

Primary Completion Date

April 30, 2025

Study Completion Date

December 31, 2025

Conditions
Syncope
Interventions
DIAGNOSTIC_TEST

syncope channel

"The procedures and investigations proposed for the etiological diagnosis of low-risk or neither high nor low syncope and included in the study are those recommended by the European Society of Cardiology.~No additional procedures, invasive or non-invasive explorations or blood sampling not provided for as part of routine care will be offered or carried out as part of the study.~The only change in practice for patients included in the syncope pathway The only change in practice concerns the grouping of patients included in the syncope pathway into a single day at a day hospital within 10 days of their emergency consultation."

DIAGNOSTIC_TEST

routine care

"The procedures and investigations proposed for the etiological diagnosis of low-risk or neither high nor low syncope and included in the study are those recommended by the European Society of Cardiology.in routine care, medical examinations are carried out by specialists such as cardiologists who do not practice in hospitals"

Trial Locations (1)

78390

centre hospitalier de Versailles, Le Chesnay

All Listed Sponsors
lead

Versailles Hospital

OTHER

NCT06503653 - Creation of a Syncope Channel for Patients Admitted to the Emergency Department for Loss of Consciousness and Not Hospitalized: Etiological Predictivity (Before/After Study) | Biotech Hunter | Biotech Hunter