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Active Not RecruitingNCT06503653

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

Status
Active Not Recruiting
Phase
N/A
Study type
Interventional
Enrollment
52 (estimated)
Sponsor
Versailles Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTsyncope channelThe 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_TESTroutine careThe 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

Timeline

Start date
2024-03-31
Primary completion
2025-04-30
Completion
2025-12-31
First posted
2024-07-16
Last updated
2025-04-10

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT06503653. Inclusion in this directory is not an endorsement.