Evaluation of the Quantra QStat System in Obstetric Patients

Sponsor
HemoSonics LLC (Industry)
Overall Status
Not yet recruiting
CT.gov ID
NCT05875987
Collaborator
(none)
50
1
9.5
5.3

Study Details

Study Description

Brief Summary

This pilot study will assess the performance of the Quantra System with the QStat Cartridge versus standard of care coagulation testing in bleeding pregnant women at delivery.

Condition or Disease Intervention/Treatment Phase
  • Device: Quantra System

Detailed Description

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 QStat Cartridge was developed to monitor hemostasis in patients that may experience a range of coagulopathies of various etiologies including fibrinolytic defects. These patients include the tobstetric hemorrhage population. The cartridge consists of four independent channels each containing different sets of reagents, which provide four measurements performed in parallel yielding five parameters that depict the functional status of a patient's coagulation system.

This single-center, prospective, observational pilot study will evaluate the performance of the Quantra System with the QStat Cartridge as compared to standard of care coagulation testing in bleeding pregnant women at delivery.

Study Design

Study Type:
Observational
Anticipated Enrollment :
50 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Pilot Study Evaluating the Clinical Performance of the Quantra With the QStat Cartridge at the Point-of-care in Obstetric Patients
Anticipated Study Start Date :
May 15, 2023
Anticipated Primary Completion Date :
Jan 31, 2024
Anticipated Study Completion Date :
Feb 28, 2024

Arms and Interventions

Arm Intervention/Treatment
Obstetric Patients

Obstetric patient population experiencing excessive bleeding around the time of delivery

Device: Quantra System
Diagnostic device to monitor coagulation properties of a whole blood sample at the point-of-care.
Other Names:
  • QStat Cartridge
  • Outcome Measures

    Primary Outcome Measures

    1. Comparison of Quantra Clot Time to laboratory aPTT test results [At the time the OB hemorrhage protocol is activated, anticipated with 24 hours after birth]

      Coagulation function assessed by Quantra Clot Time (CT, sec) and activated partial thromboplastin (aPTT, sec) test

    2. Comparison of Quantra Fibrinogen Contribution to Clot Stiffness to laboratory coagulation fibrinogen test results [At the time the OB hemorrhage protocol is activated, anticipated with 24 hours after birth]

      Coagulation function assessed by Quantra Fibrinogen Contribution to Clot Stiffness (FCS, hPa) and Clauss fibrinogen (mg/dL) test

    3. Comparison of Quantra Clot Time to ROTEM delta INTEM CT test results [At the time the OB hemorrhage protocol is activated, anticipated with 24 hours after birth]

      Coagulation function assessed by Quantra Clot Time (CT, sec) and ROTEM INTEM CT (sec) test

    4. Comparison of Quantra Fibrinogen Contribution to Clot Stiffness to ROTEM delta FIBTEM test results [At the time the OB hemorrhage protocol is activated, anticipated with 24 hours after birth]

      Coagulation function assessed by Quantra Fibrinogen Contribution to Clot Stiffness (FCS, hPa) and ROTEM FIBTEM (mm) test

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Subject is > 18 years.

    • Subject is pregnant or at least 24 h postpartum

    • Subject is fluent in English language.

    • Subject is experiencing significant bleeding resulting in activation of the stage 2 OB hemorrhage protocol as defined by blood loss ≥1500ml at delivery or within the first 24 hours after delivery, and/or is hemodynamically unstable and/or is experiencing increased abnormal bleeding not responsive to OB stage 1 hemorrhage resuscitation.

    • Subject or subject's legally authorized representative (LAR) is willing to provide informed consent, either prospectively or by deferred consent.

    Exclusion Criteria:
    • Subject is incarcerated at the time of the study.

    • Subject is currently enrolled in a distinct study that might confound the results of the proposed study

    • Subject is affected by a condition that, in the opinion of the clinical team, may pose additional risks

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Duke University Hospital Durham North Carolina United States 27710

    Sponsors and Collaborators

    • HemoSonics LLC

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    HemoSonics LLC
    ClinicalTrials.gov Identifier:
    NCT05875987
    Other Study ID Numbers:
    • HEMCS-044
    First Posted:
    May 25, 2023
    Last Update Posted:
    May 25, 2023
    Last Verified:
    May 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    Yes
    Product Manufactured in and Exported from the U.S.:
    Yes
    Keywords provided by HemoSonics LLC
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 25, 2023