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

ACTIVE_NOT_RECRUITINGNA

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

NCT06503653•Versailles Hospital

View on ClinicalTrials.gov

Summary

The main aim of this study is to assess the value of creating a "syncope pathway" to optimize diagnostic performance in patients admitted to the emergency department for syncope and not hospitalized, compared with the previous pre-syncope pathway situation.

Eligibility

Age

18 - No limit years

Sex

ALL

Healthy Volunteers

Inclusion Criteria

•Adults aged 18 and over;
•Consultant at the emergency department of the Centre Hospitalier de V ersailles
•For a confirmed diagnosis:
•of recurrent syncope with low-risk criteria according to ESC 2018 (1,2) Or
•of syncope recurrent or not, not fulfilling low-risk or high-risk criteria according to the ESC 2018 definition (1,2). These patients are those with minor high-risk criteria without aggravating circumstances:
•* With no personal history of loss of consciousness whose clinical features strongly suggest syncope of rhythmic origin;
•* No structural heart disease or abnormal ECG.
•Outpatient (returning home after emergency);
•Beneficiary or beneficiary of a social security scheme (excluding AME).

Exclusion Criteria

•Etiology of syncope identified as early as the emergency department visit;
•High-risk syncope according to ESC 2018 criteria (1,3);
•First and only episode of low-risk syncope according to ESC 2018 criteria (1,3);
•Syncope of any risk category requiring hospitalization at the discretion of the emergency physician and cardiologist;
•Legal protection by guardianship ;
•Language barrier or condition incompatible with the patient's understanding or informed adherence to the protocol;
•Opposition to the use of their pseudonymized data (for retrospective inclusions);
•Patient's refusal to give consent to participate in the study (for prospective inclusions);

Locations (1)

centre hospitalier de Versailles

Le Chesnay, Yvelines, France

Key Dates

Start Date

March 31, 2024

Primary Completion Date

April 30, 2025

Completion Date

December 31, 2025

Last Updated

April 10, 2025

Enrollment

ESTIMATED participants

Conditions

Syncope

Interventions

syncope channel

DIAGNOSTIC_TEST

routine care

DIAGNOSTIC_TEST

REmote Cardiac MOnitoring of At-risk SYNCope Patients After Emergency Department Discharge -RCT

NCT05066347

Syncope

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RECRUITINGNA

Cardioneuroablation for Reflex Syncope and Exercise Capacity

NCT06440291

Syncope, Vasovagal

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RECRUITINGNA

Cardioneuroablation: Fragmented Atrial Potentials, Intracardiac Echocardiography and Computed Tomography

NCT06472102

Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: April 10, 2025Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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

Inclusion Criteria

Exclusion Criteria

REmote Cardiac MOnitoring of At-risk SYNCope Patients After Emergency Department Discharge -RCT

Cardioneuroablation for Reflex Syncope and Exercise Capacity

Cardioneuroablation: Fragmented Atrial Potentials, Intracardiac Echocardiography and Computed Tomography

The Effect of Water Carbonation on Orthostatic Tolerance

Clinical Association Between Obstructive Sleep Apnea, Facial Pigmentation, and Vasovagal Symptoms.

Mechanism-based Therapy of Hypotensive Syncope