Evaluation of the Clinical Performance of the Quantra System With the QStat Cartridge

HemoSonics

Status

Completed

Conditions

Blood Loss Massive

Trauma

Hemorrhage, Postpartum

Treatments

Diagnostic Test: Quantra System

Study type

Observational

Funder types

Industry

Identifiers

NCT03912545

HEMCS-019

Details and patient eligibility

About

This pilot study will evaluate the performance of the Quantra System comprised of the Quantra Hemostasis Analyzer with the QStat Cartridge in trauma patients or patients with OB hemorrhage.

Full 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 trauma and obstetric hemorrhage populations. 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 coagulation tests and comparable measures using conventional viscoelastic testing methods.

Enrollment

30 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Subject is ≥ 18 years of age
Subject has one of the following conditions and is a candidate for a ROTEM test to be performed to access coagulopathy: trauma patient; patient with OB hemorrhage.
- For trauma patients; subject must be experiencing major trauma (preferably requiring the highest level of team activation) with active bleeding or deemed at high risk of significant bleeding according to mechanism of injury.
- For subjects experiencing OB hemorrhage, one of the following conditions must be met (to be confirmed):
  - Estimated blood loss during vaginal delivery is greater than 1000 mL
  - Estimated blood loss during cesarean delivery is greater than 1500 mL
  - Placental abruption with hemorrhage of any quantity blood loss
  - Clinically suspected disseminated intravascular coagulation (DIC)
  - Is under consideration for administration of tranexamic acid (TXA) for treatment of hemorrhage.
Subject is willing to participate, and is willing to consent (either prospectively or by deferred consent)

Exclusion criteria

Subject is younger than 18 years of age
Subject is known to have received antifibrinolytic therapy immediately prior to presentation to trauma unit or during labor just prior to OB hemorrhage.
Subject is unable to provide written informed consent (either prior to performing any study related procedures or by deferred consent)
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.