Comparison of the VerifyNow® Aspirin Test and PRUTest® Platelet Reactivity Tests With Investigational Reagent to Reagents Registered in Japan
Study Details
Study Description
Brief Summary
This is a multi-center convenience sample prospective study comparing the results of the Verify Now® Aspirin Test and PRUTest® Platelet Reactivity Tests with the Japan investigational reagents to reagents registered in Japan in the expected population receiving aspirin (ASA) and the P2Y12 inhibitor clopidogrel.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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Detailed Description
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The Primary Objectives of this study are to compare the results of:
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The VerifyNow Aspirin Test with AA, an investigational reagent as defined in Japan, against LTA with AA investigational reagent as defined in Japan (study reference reagent), in subjects receiving DAPT (ASA and clopidogrel or subjects taking no platelet inhibitors including ASA;
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The VerifyNow Aspirin Test with AA, an investigational reagent as defined in Japan, against LTA with collagen (study reference reagent),
o In subjects receiving DAPT (ASA and clopidogrel) or in subjects taking no platelet inhibitors including ASA
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The VerifyNow PRUTest with ADP, an investigational reagent as defined in Japan, and PGE1, against LTA with ADP, an approved reagent in Japan (study reference reagent) and PGE1, and
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The VerifyNow PRUTest with ADP (an investigational reagent as defined in Japan) and PGE1 against LTA with ADP reagent approved in Japan (study reference reagent) with no PGE1, o in up to 75 subjects receiving DAPT (ASA and clopidogrel) and in up to 55 subjects taking no platelet inhibitors (total up to 130 subjects).
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Dual Anti-Platelet Therapy (DAPT) Whole blood from patients who are currently receiving Dual Anti-Platelet Therapy (DAPT) Clopidogrel and aspirin (ASA) for a minimum of 4 weeks (on-drug) will be used to conduct antiplatelet reactivity tests using VerifyNow assay and LTA with AggRAM Aggregometer with and without PGE1. There is no drug administration or therapeutic intervention in this study. The results of platelet activation testing using VerifyNow performed in this study are not used to influence patient care. |
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| One Anti Platelet Medication Only Whole blood from patients who are currently receiving either ASA or Clopidogrel alone for a minimum of 4 weeks (on-drug) will be used to conduct antiplatelet reactivity tests using VerifyNow assay and LTA with AggRAM Aggregometer with and without PGE1. There is no drug administration or therapeutic intervention in this study. The results of platelet activation testing using VerifyNow performed in this study are not used to influence patient care. |
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| naive No medication with anti-platelet effects There is no drug administration or therapeutic intervention in this study. The results of platelet activation testing using VerifyNow performed in this study are not used to influence patient care. |
Outcome Measures
Primary Outcome Measures
- VerifyNow® PRUTest [1 day]
Correlation of AggRAM Light Transmittance Aggregometry (LTA) compared to VerifyNow PRUTest
- VerifyNow® Aspirin Test [1 day]
Correlation of AggRAM Light Transmittance Aggregometry (LTA) compared to VerifyNow Aspirin Test
- Naive [1 day]
Correlation of AggRAM Light Transmittance Aggregometry (LTA) compared to VerifyNow Aspirin Test and VerifyNow PRUTest
Eligibility Criteria
Criteria
Inclusion Criteria:
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Males and females 18 years of age or older.
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Subjects regularly taking ASA and clopidogrel, for a minimum of 4 days prior to enrollment, or subjects taking no platelet inhibitors including ASA.
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Willing to participate and able to understand the study, including their rights and any risks associated with their participation, and sign an informed consent.
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Able and willing to donate a blood sample of 15mL.
• Exclusion Criteria
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Enrolled in any other study that involves an investigational drug and/or device.
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Smoked within one hour before blood draw.
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Had caffeine within 2 hours before blood draw.
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Had meals with high fat content within 8 hours before blood draw.
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A platelet count below 92,000/µL, or above 502,000/µL for VerifyNow Aspirin Test.*
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A platelet count below 119,000/µL, or above 502,00/µL for VerifyNow PRUTest.*
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A hematocrit level below 29%, or above 56% for VerifyNow Aspirin Test.*
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A hematocrit level below 33%, or above 52% for VerifyNow PRUTest.*
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Within the past 48 hours, exposure to any of the following drugs:
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Antiplatelet/glycoprotein inhibitors [eptifibatide, tirofiban]
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Any antiplatelet drug except clopidogrel and ASA [e.g. ticagrelor, prasugrel]
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Accriva Study Site | Jacksonville | Florida | United States | 32209 |
| 2 | Accriva Study Site | Baltimore | Maryland | United States | 21215 |
Sponsors and Collaborators
- Accriva Diagnostics
Investigators
- Study Chair: Marc Rubinstein, MD, Instrumentation Laboratory
- Study Director: Michael Martin, Accrira Diagnostics / Instrumentation Laboratory
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- VFN-CSS-19-0008