Reference Range Study for the Quantra System With the QStat Cartridge in Obstetric Patients

NCT06415760 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 129

Last updated 2025-07-23

No results posted yet for this study

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

Conditions

  • Obstetric Hemostasis
  • Coagulation

Interventions

DIAGNOSTIC_TEST

Quantra System

Diagnostic device to monitor coagulation properties of a whole blood sample at the point-of-care

Sponsors & Collaborators

  • HemoSonics LLC

    lead INDUSTRY

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-05-07
Primary Completion
2025-04-01
Completion
2025-07-01
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06415760 on ClinicalTrials.gov