Reference Range Study for the Quantra Analyzer With the Quantra Surgical Cartridge
Status: | Completed |
---|---|
Conditions: | Hematology |
Therapuetic Areas: | Hematology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 4/17/2018 |
Start Date: | January 16, 2017 |
End Date: | September 28, 2017 |
This study will establish reference range intervals for the Quantra System, a next-generation
diagnostic platform that provides whole blood coagulation testing at the point-of-care.
diagnostic platform that provides whole blood coagulation testing at the point-of-care.
The Quantra System is a fully integrated and automated in vitro diagnostic device which uses
SEER Sonorheometry, an ultrasound-based technology, to characterize the viscoelastic
properties of a whole blood sample during coagulation. The Quantra Surgical Cartridge was
developed to monitor hemostasis during major surgical procedures in adult patients. The
cartridge consists of four independent channels each containing different sets of reagents,
which provide four measurements performed in parallel yielding six parameters that depict the
functional status of a patient's coagulation system. In this multi-center, prospective,
observational study, blood samples will be obtained from healthy adult volunteers to
establish a normal reference range for the test parameters measured by the Quantra System.
SEER Sonorheometry, an ultrasound-based technology, to characterize the viscoelastic
properties of a whole blood sample during coagulation. The Quantra Surgical Cartridge was
developed to monitor hemostasis during major surgical procedures in adult patients. The
cartridge consists of four independent channels each containing different sets of reagents,
which provide four measurements performed in parallel yielding six parameters that depict the
functional status of a patient's coagulation system. In this multi-center, prospective,
observational study, blood samples will be obtained from healthy adult volunteers to
establish a normal reference range for the test parameters measured by the Quantra System.
Inclusion Criteria:
- Subject is > 18 years
- Subject is willing to participate and he/she has signed a consent form
- Subject's laboratory coagulation test results at screening are within each test's
normal reference range
Exclusion Criteria:
- Subject is younger than 18 years
- Subject has a history of a coagulation disorder
- Subject is pregnant or lactating
- Subject is currently taking medications known to alter coagulation
- Subject had a blood transfusion or surgery within the last month
- Subject has one or more laboratory coagulation test result outside of the normal
reference range at screening
- Drug abuse
- Excessive alcohol consumption
- Subject is unable to provide written informed consent
- Subject is incarcerated at the time of the study
- Subject previously participated in this study
We found this trial at
3
sites
171 Ashley Avenue
Charleston, South Carolina 29425
Charleston, South Carolina 29425
843-792-1414

Principal Investigator: Charles Greenberg, MD
Medical University of South Carolina The Medical University of South Carolina (MUSC) has grown from...
Click here to add this to my saved trials

22 S Greene St
Baltimore, Maryland 21201
Baltimore, Maryland 21201
(410) 328-8667

Principal Investigator: Kenichi Tanaka, MD
University of Maryland Medical Center Founded in 1823 as the Baltimore Infirmary, the University of...
Click here to add this to my saved trials

Click here to add this to my saved trials
