Study of Rivaroxaban Use and Potential Adverse Outcomes in Routine Clinical Practice (Germany)

CompletedOBSERVATIONAL
Enrollment

665,533

Participants

Timeline

Start Date

December 22, 2011

Primary Completion Date

September 30, 2020

Study Completion Date

September 30, 2020

Conditions
Venous ThrombosisPulmonary EmbolismAtrial FibrillationAcute Coronary Syndrome
Interventions
DRUG

Rivaroxaban (Xarelto, Bay59-7939)

"The treatment of DVT or PE, and prevention of recurrent DVT and PE in adult patients (15 mg rivaroxaban twice daily \[bid\] for 3 weeks, then 15 mg or 20 mg once daily \[od\], tablets).~The prevention of stroke and systemic embolism in adult patients with non-valvular atrial fibrillation (stroke prevention in atrial fibrillation \[SPAF\]) with one or more risk factors (20 mg rivaroxaban \[od\], tablets).~The prevention of venous thromboembolism (VTE) in adult patients undergoing elective hip or knee replacement surgery (recommended dose: 10 mg rivaroxaban \[od\] tablets for 35 days following hip replacement surgery and 14 days following knee replacement surgery).~Co-administered with acetylsalicylic acid (ASA) alone or with ASA plus clopidogrel or ticlopidine, for the prevention of atherothrombotic events in adult patients after an acute coronary syndrome (ACS) with elevated cardiac biomarkers (recommended dose 2.5 mg rivaroxaban tablets \[bid\])."

DRUG

Standard of care

For DVT/PE treatment and SPAF, standard of care is treatment with the most widely used vitamin K antagonist, phenprocoumon, and for the secondary prevention of ACS, standard of care is antiplatelet drug(s) such as low-dose acetylsalicylic acid, clopidogrel, dipyridamole, prasugrel, ticlopidine and ticagrelor.

Trial Locations (1)

Unknown

Multiple Locations

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

Janssen Research & Development, LLC

INDUSTRY

lead

Bayer

INDUSTRY

NCT01947959 - Study of Rivaroxaban Use and Potential Adverse Outcomes in Routine Clinical Practice (Germany) | Biotech Hunter | Biotech Hunter