About this trial
To assess the rates of ischemic and hemorrhagic complications of long-term antithrombotic therapy in patients with atrial fibrillation
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Documented atrial fibrillation with CHA2DS2VASC > 1
Disqualifiers
Subjects who are unwilling or unable to provide informed consent. ACS within 12 months before inclusion Severe CHF (NYHA IV) Stroke within 6 months before inclusion Severe liver or muscle disease Severe kidney disease / renal failure with creatinine > 3 mg/dl Conceivable impossibility to come in touch with the patient or his family at 1-year after the intervention
Trial population
Hospitalized or outpatients with confirmed atrial fibrillation and CHA2DS2VASC \> 1
Trial design
Cohort
Prospective
Treatments tested in this trial
Anticoagulants
Drugoral anticoagulants, dual or triple antithrombotic theraphy
Treatment groups
Trial outcomes
Primary outcomes
composite of major cardiovascular events
stroke, myocardial infarction, stent thrombosis \[definite or probable\], or urgent revascularization, cqrdiac death
composite of any bleeding events
major, clinically relevant nonmajor, minor (BARC, ISTH,GARFIELD AF)
Secondary outcomes
Mutations in following genes
CYP2C9\*, VKORC1
Sponsors and contacts
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