Status:

ACTIVE_NOT_RECRUITING

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

Lead Sponsor:

Versailles Hospital

Conditions:

Syncope

Eligibility:

All Genders

18+ years

Phase:

NA

Brief 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, ...

Eligibility Criteria

Inclusion

  • 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

  • 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);

Key Trial Info

Start Date :

March 31 2024

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

December 31 2025

Estimated Enrollment :

52 Patients enrolled

Trial Details

Trial ID

NCT06503653

Start Date

March 31 2024

End Date

December 31 2025

Last Update

April 10 2025

Active Locations (1)

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1

centre hospitalier de Versailles

Le Chesnay, Yvelines, France, 78390