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PAREPET-II
Protocol: STUDY00000625
Full Title
Prediction of ARrhythmic Events with Positron Emission Tomography-II (PAREPET-II)
Description
This is a research study which will determine whether a series of tests can predict the
likelihood that your implantable cardiac defibrillator, or ICD, will deliver therapy for a dangerous heart rhythm.

If you choose to participate you will have one initial visit then we will follow-up with you by phone every three months for up to 5 years to check on your heart symptoms.

Study Visits will be in the UB Clinical and Translational Research Center, Downtown Buffalo.

Compensation is available. Your time and effort will be partially compensated by a
$60 gift card which you will receive after all testing is completed to cover the expense of
transportation and parking.
Compensation: No
Eligibility
• Coronary artery disease (by cardiac catheterization or definite myocardial infarction)
• ICD implantation for the primary prevention of SCA
• Optimal medical therapy for heart failure [angiotensin converting enzyme inhibitor (ACEI) or angiotensin receptor antagonist (ARA)].
Age Group: Adults
Principal Investigator: JOHN CANTY
ClinicalTrials.gov: Open Study
Contact(s)
JOHN CANTY
canty@buffalo.edu
+1 716-829-2663
Natalie Stafford
nstaffor@buffalo.edu
+1 716-829-6115
Want to Learn More?

Let us know how the study team can reach you. If you do not hear back within 2 business days, then reach out to the study team directly at the contact information above and someone will assist you.

Your information will be shared only with the research study team and administrative staff for recruitment and will remain confidential. Your information will be stored until study recruitment is closed. Should you no longer want this information to be provided in the aforementioned ways, please contact the study team directly.

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