Xarelto Regulatory Post-Marketing Surveillance

Status Completed

Clinical Trial Summary

This study is to identify the following problems and questions with respect to the safety and effectiveness of Xarelto in comparison with other pharmacologic agents in the prophylaxis of venous thromboembolism (VTE) in a large sample of patients who undergo elective total hip replacement (THR) or total knee replacement (TKR) in the real-life conditions in its registered indication(s) as required by Korean Food and Drug Administration (KFDA).

1. Known and unknown adverse reactions, especially serious adverse reactions

2. Incidence of adverse reactions under the routine drug use

3. Factors that may affect the safety of the drug

4. Factors that may affect the effectiveness of the drug

5. Other safety information related to overuse, drug interaction and laboratory abnormalities

6. Other adverse reactions

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01029743
Study type	Observational
Source	Bayer
Contact
Status	Completed
Phase	N/A
Start date	December 2009
Completion date	January 2016

View Details

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