Heparin-Induced Thrombocytopenia Clinical Trial
Official title:
A Phase II Trial Using Fondaparinux in Patients With Confirmed or Suspected Heparin-Induced Thrombocytopenia (HIT)
The purpose of this study is to determine how safe and effective fondaparinux is in treating patients with suspected or confirmed heparin-induced thrombocytopenia (HIT).
Currently, standard treatment of HIT involves the transition from a direct thrombin inhibitor
(a type of anticoagulant or "blood thinner") to warfarin, a different type of anticoagulant.
Direct thrombin inhibitors (DTIs) require IV administration and frequent blood draws for dose
adjustments, which can lead to prolonged hospitalization. DTIs also affect blood test
measurements, making it difficult to determine proper dosages of warfarin.
Fondaparinux is a drug that is approved by the FDA for the treatment of blood clots in deep
veins and in the lungs. Fondaparinux is not FDA approved for the treatment of HIT. However,
an increasing number of doctors are using fondaparinux instead of DTIs to treat HIT. Although
fondaparinux appears to be more convenient and predictable than DTI medications, more
research is needed to support its use as a treatment for HIT.
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