Venous Thromboembolism Clinical Trial
Official title:
Plasma Anti-FXa Concentration After Continuous Intravenous Infusion and Subcutaneous Dosing of Enoxaparin for Thromboprophylaxis in Critically Ill Patients
To evaluate the pharmacokinetics of the thromboprophylactic agent enoxaparin in critically
ill patients by comparing plasma anti-factor Xa activity when enoxaparin is administered
either as a continuous intravenous infusion or subcutaneous bolus once daily.
To investigate possible ongoing coagulation by coagulation markers during antithrombotic
therapy with standard doses of enoxaparin
n/a
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