Study Type
Inteventional - Drug
The objective of ASPIRE-AF is to assess the effects of non-vitamin K oral anticoagulants (NOACs) versus no anticoagulation on the co-primary composite outcomes of:
1. non-hemorrhagic stroke and systemic embolism, and
2. vascular mortality, and non-fatal non-hemorrhagic stroke, myocardial infarction, peripheral arterial thrombosis, amputation, and symptomatic venous thromboembolism
over the duration of follow-up in patients with atrial fibrillation (AF) occurring transiently with stress (AFOTS) like non-cardiac surgery and acute illness.
About ASPIRE-AFInteventional - Drug
Prospective, randomized, open-label clinical trial with blinded outcome assessment
20
130
2270
2019 - 2030
PHRI
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