25
Participants
Start Date
May 31, 2009
Primary Completion Date
May 31, 2011
Study Completion Date
June 30, 2011
Rivaroxaban (Xarelto, BAY59-7939)
Participants received 30 mg rivaroxaban bid (twice-daily) orally for the first 3 weeks followed by 20 mg rivaroxaban bid for the remainder of the 3-month treatment period.
Vienna
Roodepoort
Johannesburg
Johannesburg
Redcliffe
Debrecen
Worcester
Somerset West
Pavia
Holon
München
Ashkelon
São Paulo
Amsterdam
Pretoria
Pretoria
Lead Sponsor
Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
INDUSTRY
Bayer
INDUSTRY