University Hospital of Heidelberg
Heidelberg, Baden-Wurttemberg, 69120, Germany
NCT Number: NCT05995561
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
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Notify Me18 year and older
All sexes
Observational
Heidelberg, Baden-Wurttemberg, 69120, Germany
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
no intervention is planned.
Time frame: 24 months
all-cause mortality during follow-up
Time frame: 24 months
ischaemic stroke during follow-up
Time frame: 24 months
major bleeding during follow-up
Time frame: 24 months
myocardial infarction during follow-up
University Hospital Heidelberg
Other
Heidelberg Registry of Atrial Fibrillation
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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