Xarelto [SPAF] Post-marketing Surveillance in Japan

Status Completed

Clinical Trial Summary

This study is a regulatory post-marketing surveillance in Japan, and it is a local prospective and observational study of patients who have received Xarelto for SPAF. The objective of this study is to assess safety and effectiveness of Xarelto using in real clinical practice. A total of 10,000 patients are to be enrolled and assessed in 2 years standard observational period. An annual follow-up survey will be conducted for 5 years at the longest after standard observational period.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01582737
Study type	Observational
Source	Bayer
Contact
Status	Completed
Phase
Start date	May 30, 2012
Completion date	January 17, 2020

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