This is a multi-center study designed to evaluate the accuracy and precision of the INRatio® Prothrombin Time (PT) Monitoring System, utilizing the INRatio test strip newly designed for low sample volume and heparin insensitivity, when used by trained medical professionals for the quantitative determination of PT and International Normalized Ratio (INR) in fingerstick and venous whole blood from subjects on oral anticoagulation therapy (OAT). These results will be compared to those PT/INR results obtained on plasma from the same subjects as analyzed at a central laboratory with the Sysmex CA-560 System.
Study Type
OBSERVATIONAL
Enrollment
271
Loma Linda VA Hospital
Loma Linda, California, United States
UC Davis Healthcare System
Sacramento, California, United States
San Diego Cardiac Center
San Diego, California, United States
Fox Valley Cardiology
Aurora, Illinois, United States
Analytical accuracy and precision of the INRatio Prothrombin Time (PT) Monitoring System.
Time frame: 3-6 months
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