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Clinical Trial Summary

The overall goal of this study was to evaluate the comparative safety and effectiveness of rivaroxaban vs. vitamin K antagonist (VKA) for stroke prevention in patients with nonvalvular atrial fibrillation (NVAF) across risk profiles and comorbidities that reflect everyday clinical practice.

The primary objective in this study was to evaluate the combined end point of stroke or systemic embolism (SSE), and major bleeding in NVAF patients treated with rivaroxaban vs. VKA.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03374540
Study type Observational
Source Bayer
Contact
Status Completed
Phase
Start date December 1, 2017
Completion date August 30, 2019

See also
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