Management of Transitory Loss of Consciousness and Syncopes in the Emergency Department

Syncope Clinical Trial

Official title:

Management of Transitory Loss of Consciousness and Syncopes in the Emergency Department

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05575934
• Other study ID #: EI22MG0908
• Status: Recruiting
• Start date: October 3, 2022
• Est. completion date: September 30, 2023

Study information

• Verified date: October 2022
• Source: University Hospital, Clermont-Ferrand
• Contact: Lise Laclautre
• Phone: 334.73.754.963
• Email: promo_interne_drci[@]chu-clermontferrand.fr
• Is FDA regulated: No
• Study type: Observational

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

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.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 250
• Est. completion date: September 30, 2023
• Est. primary completion date: March 25, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• patients over 18 presenting to the Clermont-Ferrand University Hospital emergency department for transient loss of consciousness of syncopal or undifferentiated origin

Exclusion Criteria:

• N/A

Related Conditions & MeSH terms

• Emergencies
• Syncope
• Unconscious State
• Unconsciousness

Locations

Country	Name	City	State
France	CHU Clermont-Ferrand	Clermont-Ferrand

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital, Clermont-Ferrand

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	prevalence of transient loss of consciousness in emergency department	Percentage of TLOC in emergency department	through the study duration, an average of 6 months
Primary	prevalence of different diagnoses leading to transient loss of consciousness	Percentage of different diagnoses leading to transient loss of consciousness	through the study duration, an average of 6 months
Secondary	prevalence of different clinical presentations of loss of consciousness	Percentage of different clinical presentations of loss of consciousness	through the study duration, an average of 6 months
Secondary	Prevalence of the various diagnostic tests carried out and the treatment of patients presenting for transient loss of consciousness	Percentage of the various diagnostic tests carried out and the treatment of patients presenting for transient loss of consciousness	through the study duration, an average of 6 months