72
Participants
Start Date
February 3, 2022
Primary Completion Date
August 31, 2028
Study Completion Date
August 31, 2028
"treatment intervention"
for a total of 12 weeks, prophylactic heparin therapy during hospitalization followed by prophylactic oral anticoagulation with apixaban
"treatment standard"
during hospitalization prophylactic heparin therapy followed by management without prophylactic anticoagulation.
biological assessment
CBC, reticulocytes, haptoglobin, LDH, bilirubin
RECRUITING
Chu Dijon Bourgogne, Dijon
Centre Hospitalier Universitaire Dijon
OTHER