120
Participants
Start Date
November 4, 2024
Primary Completion Date
October 31, 2026
Study Completion Date
October 31, 2026
Rivaroxaban 10 MG
The intervention in the experimental arm will be rivaroxaban, 10 mg PO once daily (prophylactic dosing) for 180 days after the start of systemic therapy or until one of the primary study outcomes occurs (VTE or major bleeding).
Placebo control
Identical to Rivaroxaban intervention except participants will receive a matched placebo instead of the study drug
RECRUITING
Ottawa Hospital Research Institute, Ottawa
Lead Sponsor
Canadian Institutes of Health Research (CIHR)
OTHER_GOV
Canadian Venous Thromboembolism Clinical Trials and Outcomes Research (CanVECTOR) Network
NETWORK
Kidney Cancer Research Network of Canada
UNKNOWN
Ottawa Hospital Research Institute
OTHER