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Clinical Trial Summary

This study will determine reference range intervals for the parameters reported by the Quantra System with the QStat Cartridge in the last trimester of non-laboring pregnant women with an uncomplicated pregnancy


Clinical Trial Description

During pregnancy, there is a progressive shift of hemostasis toward a hypercoagulable state that is protective against postpartum hemorrhage. To assess the clinical utility of the Quantra System in high-risk OB patients during delivery, it is important to understand how the normal physiological changes of pregnancy impact Quantra results. This study will determine reference range intervals for the parameters reported by the Quantra System with the QStat Cartridge in the last trimester of non-laboring pregnant women with an uncomplicated pregnancy. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06415760
Study type Observational
Source HemoSonics LLC
Contact
Status Enrolling by invitation
Phase
Start date May 7, 2024
Completion date October 31, 2024

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