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AFHRI is planned as a prospective, single-center cohort study in patients at high risk of AF.
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The primary aim of the study is to evaluate and improve atrial fibrillation risk prediction, which takes into account clinical, psycho-social, environmental and lifestyle-risk factors, protein patterns and genetic variability in addition to the classical risk factors with respect to the primary endpoint, AF (paroxysmal or permanent).
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Central trial contact
Renate B Schnabel, Prof.; Daniel Engler, MSc.
Data sourced from clinicaltrials.gov
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