Thrombocyte Activity Reassessment and GEnoTyping for PCI(TARGET-PCI)

NATerminatedINTERVENTIONAL
Enrollment

7

Participants

Timeline

Start Date

July 31, 2010

Primary Completion Date

October 31, 2010

Study Completion Date

October 31, 2010

Conditions
Coronary Artery Disease
Interventions
DEVICE

VerifyNow, Verigene

Subjects on chronic clopidogrel will be guided by VerifyNow P2Y12 assay, whereas clopidogrel naïve subjects will be guided by Verigene CYP2C19 genotyping assay. Patients on clopidogrel maintenance and/or in the control group will also be genotyped; conversely, clopidogrel naïve subjects will have VerifyNow testing prior to discharge for additional study analysis. Patients in the guided therapy group that have a measurement of ≥ 230 PRU will be reloaded with 60mg prasugrel and receive standard maintenance dosing. Similarly, clopidogrel naïve subjects that are considered CYP2C19\*2 carriers will also be reloaded with 60mg prasugrel and receive standard maintenance dosing (see flow schematic).

Trial Locations (1)

21215

Sinai Center for Thrombosis Research, Baltimore

Sponsors

Lead Sponsor

All Listed Sponsors
lead

LifeBridge Health

OTHER

NCT01177592 - Thrombocyte Activity Reassessment and GEnoTyping for PCI(TARGET-PCI) | Biotech Hunter | Biotech Hunter