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