A randomised clinical trial investigating the effect of edoxaban versus dalteparin in patients with cancer who had acute symptomatic or incidental venous thromboembolism
Studied treatment | low-molecular-weight heparin for at least 5 days followed by oral edoxaban at a dose of 60 mg once daily. Treatment was given for atleast 6 months and up to 12 months. |
Control treatment | subcutaneous dalteparin at a dose of 200 IU per kilogram of body weight once daily for 1 month followed by dalteparin at a dose of 150 IU per kilogram once daily |
Patients | patients with cancer who had acute symptomatic or incidental venous thromboembolism |
Group sizes | 522 / 524 |
Blindness | open label | Inclusion period | |
Follow-up duration | Centers | ||
Lost to FU | geographical localisation | ||
Primary endpoint | recurrent venous thromboembolism or major bleeding at12 months | Design |
Raskob GE Edoxaban for the Treatment of Cancer-Associated Venous Thromboembolism. N Engl J Med 2018;378:615-624 [PMID: 29231094] link to pdf add to Mendeley
ClinicalTrial.gov record NCT02073682
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