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Clinical Trial Summary

The primary objectives of this study are: - To estimate the incidence rate of unexpected adverse events - To characterize the bleeding events and assess risk factors of bleeding - To identify ancillary baseline variables that may also be associated with adverse outcomes


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02007655
Study type Observational
Source Bristol-Myers Squibb
Contact
Status Completed
Phase
Start date September 1, 2013
Completion date August 31, 2016

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