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NCT05995561 Clinical Trial

HERA FIb Registry for Patients With Atrial Fibrillation

Atrial Fibrillation Clinical Trial

Official title:
Heidelberg Registry of Atrial Fibrillation

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05995561
Other study ID # HERA FIb registry
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 1, 2009
Est. completion date April 1, 2020

Study information
Verified date May 2024
Source University Hospital Heidelberg
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The single-center HERA AFIb registry was created to assess real-world prevalence, demographic characteristics and management of patients with atrial fibrillation (AF) in the era of novel oral anticoagulant regimes (NOAC) presenting in the emergency department (ED) of University of Heidelberg

Description:

HERA AFIb is a single-center retrospective registry which enrolled consecutive cases presenting with atrial fibrillation at the emergency department of University Hospital of Heidelberg. Clinical parameters and characteristics for cases were assessed retrospectively. Follow-up was performed via review of medical reports, phone calls and postal queries. Outcome parameters included rates for all-cause mortality, non-hemorrhagic stroke, myocardial infarction and major bleeding.

Recruitment information / eligibility
Status Completed
Enrollment 12297
Est. completion date April 1, 2020
Est. primary completion date April 1, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - documented atrial fibrillation - availability of at least one hsTnT measurement Exclusion Criteria: - lost to follow-up

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• no intervention is planned.
no intervention is planned.

Locations
Country Name City State
Germany University Hospital of Heidelberg Heidelberg Baden-Württemberg

Sponsors (1)
Lead Sponsor Collaborator
University Hospital Heidelberg

Country where clinical trial is conducted

Germany, 

Outcome
Type Measure Description Time frame Safety issue
Primary all-cause mortality all-cause mortality during follow-up 24 months
Secondary ischaemic stroke ischaemic stroke during follow-up 24 months
Secondary major bleeding major bleeding during follow-up 24 months
Secondary myocardial infarction myocardial infarction during follow-up 24 months
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