Clinical Assessment Transient Loss of Consciousness

• Conditions: R55; R40; Syncope and collapse; Somnolence, stupor and coma

• Registration Number: DRKS00026002
• Lead Sponsor: niversitätsklinikum Essen

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2021-08-06
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 250

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

-Minors (< 18 years)
-Non-consenting adults (e.g., acutely intoxicated, legal guardian not present).
-known epilepsy
-Direct association of the event with previous trauma

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Syncope Risk Stratification

Secondary Outcome Measures

Name	Time	Method
Description of the treatment pathways in the follow-up with regard to outcome and adverse events<br>Deriving a matrix for subsequent, more recent studies