Overview

Thrombelastography Based Dosing of Enoxaparin

Status:
Completed
Trial end date:
2015-03-01
Target enrollment:
Participant gender:
Summary
The risk of developing a blood clot occurs in up to 60% of all critical care patients. Many times enoxaparin (or Lovenox®) is given to patients who are at a higher risk of developing clots in their legs or lungs. Recent data suggest that a standard dose of Lovenox may not fully prevent the development of these clots especially in critically ill or obese patients. Routine enoxaparin dosing can also result in bleeding complications. Thrombelastography (TEG®) can be used to measure how blood clots. The purposes of this study are: - to learn if the TEG® can better guide physicians in prescribing an effective dose of Lovenox compared to standard doses recommended by the drug company in preventing blood clots from developing in the legs and lungs, and - to compare the development of blood clots in patients receiving the standard dose of enoxaparin compared to patients receiving a TEG® guided dose of enoxaparin. - to determine if TEG guided dosing results in decreased bleeding complications compared to standard dosing.
Phase:
N/A
Details
Lead Sponsor:
Oregon Health and Science University
Collaborators:
Medical Research Foundation, Oregon
National Trauma Institute
National Trauma Research Institute
Treatments:
Enoxaparin
Enoxaparin sodium