Evaluation of coagulation results reported by the Qplus Quantra System to determine pediatric reference range intervals.
Single center observational study of the pediatric patient population (\< 18yrs) with normal coagulation function to determine the reference range interval for the clotting parameters reported by the Quantra QPlus system.
Study Type
OBSERVATIONAL
Enrollment
93
Diagnostic device to monitor coagulation properties of a whole blood sample at the point of care
Nicklaus Childrens Hospital
Miami, Florida, United States
Reference range interval for measurement of clot time (CT) parameter
Reference range interval determined in this study will serve as the reference for CT results in this particular population
Time frame: Baseline, after access placement before any procedures
Reference range interval for measurement of clot time (CTH) parameter
Reference range interval determined in this study will serve as the reference for CTH results in this particular population
Time frame: Baseline, after access placement before any procedures
Reference range interval for measurement of clot stiffness (CS) parameter
Reference range interval determined in this study will serve as the reference for CS results in this particular population
Time frame: Baseline, after access placement before any procedures
Reference range interval for measurement of Fibrinogen Contribution to clot stiffness (FCS) parameter
Reference range interval determined in this study will serve as the reference for FCS results in this particular population
Time frame: Baseline, after access placement before any procedures
Reference range interval for measurement of Platelet Contribution to clot stiffness (PCS) parameter
Reference range interval determined in this study will serve as the reference for PCS results in this particular population
Time frame: Baseline, after access placement before any procedures
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