Evaluation of the Clinical Performance of the Quantra System With the QStat Cartridge
Study Details
Study Description
Brief Summary
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.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
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 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.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Trauma patients Subjects experiencing major trauma such that viscoelastic testing is performed as standard of care to assess coagulopathy. |
Diagnostic Test: Quantra System
Diagnostic device to monitor coagulation properties of a whole blood sample at the point-of-care.
Other Names:
|
| Obstetric hemorrhage patients Subjects experiencing obstetric hemorrhage such that viscoelastic testing is performed as standard of care is performed to assess coagulopathy. |
Diagnostic Test: Quantra System
Diagnostic device to monitor coagulation properties of a whole blood sample at the point-of-care.
Other Names:
|
Outcome Measures
Primary Outcome Measures
- Comparison of Quantra Clot Time and Clot Stiffness results to standard coagulation test results [Upon arrival to emergency department (trauma subjects) or upon presentation with obstetric hemorrhage, prior to the administration of blood products or antifibrinolytics in parallel with samples collected for routine ROTEM analysis and laboratory assays]
Coagulation function assessed by Quantra and standard coagulation tests
- Comparison of Quantra Clot Time and Clot Stiffness results to ROTEM Delta results [Upon arrival to emergency department (trauma subjects) or upon presentation with OB hemorrhage, prior to the administration of blood products or antifibrinolytics in parallel with samples collected for routine ROTEM analysis and laboratory assays]
Coagulation function assessed by Quantra and ROTEM Delta
- Comparison of Quantra Fibrinolysis results to ROTEM Delta results [Upon arrival to emergency department (trauma subjects) or upon presentation with OB hemorrhage, prior to the administration of blood products or antifibrinolytics in parallel with samples collected for routine ROTEM analysis and laboratory assays]
Coagulation function assessed by Quantra and ROTEM Delta
Eligibility Criteria
Criteria
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.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Texas Tech University Health Sciences Center El Paso | El Paso | Texas | United States | 79905 |
Sponsors and Collaborators
- HemoSonics LLC
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- HEMCS-019