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Be Part of Research - Trial Details - The Management of Transient Loss of Consciousness and Suspected Syncope in European Emergency Departments
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The Management of Transient Loss of Consciousness and Suspected Syncope in European Emergency Departments

Completed

Open to: ALL

Age: 18.0 - N/A

Edinburgh Coventry Kirkcaldy Livingston Preston

Medical Conditions

Syncope

This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.


Prospective multi centre cohort study examining the clinical presentation, diagnostic tests, and management of adult Emergency Department (ED) patients presenting with Transient Loss of Consciousness (TLOC) either undifferentiated or thought to be of syncopal origin.

Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.  

The recruitment start and end dates are as follows:

Sep 2022 Dec 2022

Publications

"Reed MJ, Karuranga S, Kearns D, Alawiye S, Clarke B, Mockel M, Karamercan M, Janssens K, Riesgo LG, Torrecilla FM, Golea A, Fernandez Cejas JA, Lupan-Muresan EM, Zaimi E, Nuernberger A, Rennet O, Skjaerbaek C, Polyzogopoulou E, Imecz J, Groff P, Camilleri R, Cimpoesu D, Jovic M, Miro O, Anderson R, Laribi S; SEED investigators. Management of syncope in the Emergency Department: a European prospective cohort study (SEED). Eur J Emerg Med. 2024 Apr 1;31(2):136-146. doi: 10.1097/MEJ.0000000000001101. Epub 2023 Nov 27."; "38015745"

OBSERVATIONAL

Intervention Type : OTHER
Intervention Description : All patients will have a focussed Case Report Form completed collecting routine data describing the prevalence, clinical presentation, assessment, management and ESC risk category of patients, at the time or shortly after the patients ED attendance.




You can take part if:



You may not be able to take part if:


This is in the inclusion criteria above


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.

  • Royal Infirmary of Edinburgh
    Edinburgh
    Midlothian
    EH16 4SA
  • University Hospital Coventry & Warwickshire
    Coventry
  • Victoria Hospital
    Kirkcaldy
  • St Johns Hospital, Livingston
    Livingston
  • Royal Preston Hospital
    Preston


The study is sponsored by NHS Lothian



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Read full details for Trial ID: NCT05571254
Last updated 22 March 2023

This page is to help you find out about a research study and if you may be able to take part

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