Venous Thromboembolism Clinical Trial
Official title:
Multicenter, Randomized, Parallel-group Efficacy and Safety Study for the Prevention of Venous Thromboembolism in Hospitalized Medically Ill Patients Comparing Rivaroxaban With Enoxaparin. The MAGELLAN Study
This study will evaluate if extended therapy with oral rivaroxaban can prevent blood clots in the leg and lung that can occur with patients hospitalized for acute medical illness, and compare these results with those of the standard enoxaparin dose and duration regimen. The safety of rivaroxaban will also be studied.
The treatment period was followed by a follow-up period starting the day after the last
intake of study medication, regardless of the actual duration of study drug administration
and ended on Day 90 (+ 7 days). Participants who did not complete the treatment period also
entered the follow-up period. It was also possible that participants did not enter the
follow-up period, e.g. due to withdrawal of consent or termination of study participation.
Within the US 'Johnson & Johnson Pharmaceutical Research & Development, L.L.C.' is sponsor.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention
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