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Clinical Trial Summary

The objective of this regulatory Post-Marketing Surveillance in Korea is to reconfirm the clinical usefulness of Eliquis through collecting, reviewing, identifying and verifying the safety and effectiveness information about Eliquis in general practice


Clinical Trial Description

n/a


Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT01885585
Study type Observational
Source Bristol-Myers Squibb
Contact
Status Completed
Phase N/A
Start date July 2014
Completion date May 2015

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