R55 R40
Conditions
Interventions
Group 1: Patients are recruited on the basis of the referral diagnosis or triage diagnosis in the Central Emergency Department North of the University Medical Center Essen.
Study data collection is p
Sponsors
Universitätsklinikum Essen
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: -Presentation in the ZNA North of the University Hospital Essen after having experienced a temporary loss of consciousness and -age of majority (=18 years) -ability to give consent (patient is able to understand the nature, significance, and scope of the medical data collection measure)
Exclusion criteria
Exclusion criteria: -Minors (< 18 years) -Non-consenting adults (e.g., acutely intoxicated, legal guardian not present). -known epilepsy -Direct association of the event with previous trauma
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Syncope Risk Stratification | — |
Secondary
| Measure | Time frame |
|---|---|
| Description of the treatment pathways in the follow-up with regard to outcome and adverse events Deriving a matrix for subsequent, more recent studies | — |
Countries
Germany
Contacts
Public ContactJoachim Riße
Uniklinik Essen
Outcome results
None listed