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OpenTrials
Completed

NCT Number: NCT03685097

Comparison of Two Point-of-care Devices for Viscoelastic Hemostasis Assays

This study will investigate the correlation and agreement of Quantra-derived parameters with parameters reported by the ROTEM delta and standard laboratory tests in cardiac surgery patients. In addition the association of Quantra-derived parameters with select platelet function tests will be investigated.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

IRCCS Policlinico San Donato

Milan, Italy

About this study

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 QPlus Cartridge (previously called the Surgical Cartridge), was developed to monitor hemostasis during major surgical procedures in adult patients. The cartridge provides six parameters that depict the functional status of a patient's coagulation system.

This single site, prospective observational study will investigate the correlation and agreement of Quantra-derived parameters with parameters reported by the ROTEM delta and standard laboratory tests (PT, aPTT, fibrinogen, platelet count) in cardiac surgery patients. As an additional exploratory study, the association of Quantra-derived parameters with select platelet function tests will be investigated.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subject is >18 years
  • Subject is undergoing elective cardiac surgery with cardiopulmonary bypass
  • Subject is willing to participate and has signed a consent form

Exclusion criteria

  • Subject is younger than 18 years
  • Subject has known congenital coagulopathy
  • Subject is unable to provide written informed consent

Treatment and study plan

Quantra System with the QPlus Cartridge

Diagnostic Test

Point-of-care viscoelastic testing

Primary outcomes

  1. Comparison of QPlus Clot Time and Clot Stiffness results to comparable ROTEM delta results

    Time frame: Baseline (before surgery)

    Coagulation function assessed by Quantra QPlus Cartridge and ROTEM delta

  2. Comparison of QPlus Clot Time and Clot Stiffness results to comparable ROTEM delta

    Time frame: After cardiac bypass (10 minutes after administration of protamine)

    Coagulation function assessed by Quantra QPlus Cartridge and ROTEM delta

  3. Comparison of QPlus Clot Time and Clot Stiffness results to standard coagulation test results

    Time frame: Baseline (before surgery)

    Coagulation function assessed by Quantra QPlus Cartridge and standard coagulation tests

  4. Comparison of QPlus Clot Time and Clot Stiffness results to standard coagulation test results

    Time frame: After cardiac bypass (10 minutes after administration of protamine)

    Coagulation function assessed by Quantra QPlus Cartridge and standard coagulation tests

Secondary outcomes

  1. Comparison of QPlus Clot Stiffness results to platelet function tests with multiple electrode aggregometry (MEA): ADPtest and TRAPtest

    Time frame: Baseline (before surgery)

    Platelet function assessed by Quantra QPlus Cartridge and MEA

  2. Comparison of QPlus Clot Stiffness results to platelet function tests with multiple electrode aggregometry (MEA): ADPtest and TRAPtest

    Time frame: After cardiac bypass (10 minutes after administration of protamine)

    Platelet function assessed by Quantra QPlus Cartridge and MEA

Sponsors and collaborators

Lead sponsor

HemoSonics LLC

Industry

Collaborators

  • IRCCS Policlinico S. Donato

Registry information

Important dates

Study start
2018
Primary completion
2018
Study completion
2018
First posted
Sep 26, 2018
Registry last updated
Sep 26, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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