60
Participants
Start Date
March 31, 2012
Primary Completion Date
December 31, 2013
Study Completion Date
January 31, 2014
Rivaroxaban (Xarelto, BAY59-7939)
10 mg twice daily for 21 days, followed by 15 mg once daily
Rivaroxaban (Xarelto, BAY59-7939)
15 mg twice daily for 21 days, followed by 15 mg once daily
Unfractionated heparin
To be adjusted to maintain the activated partial thromboplastin time (aPTT) prolongation (1.5 to 2.5 times the control)
Warfarin
To be adjusted on the basis of prothrombin time-international normalized ratio (PT-INR) values target range (1.5 to 2.5)
Toyoake
Aomori
Sakura
Fukuoka
Maebashi
Ōtake
Sapporo
Takarazuka
Kahoku-gun
Kanazawa
Yokohama
Kumamoto
Tsu
Sasebo
Niigata
Okayama
Osaka
Osaka
Sayama
Suita
Shizuoka
Tokushima
Bunkyo-ku
Chuoku
Itabashi-ku
Meguro-ku
Shinagawa
Shinjuku-ku
Wakayama
Lead Sponsor
Janssen Scientific Affairs, LLC
INDUSTRY
Bayer
INDUSTRY