Summary

Eligibility
for people ages 18 years and up (full criteria)
Location
at Los Angeles, California
Dates
study started
study ends around
Principal Investigator
by Rene R. Sevag Packard, MD, PhD
Headshot of Rene R. Sevag Packard
Rene R. Sevag Packard

Description

Summary

This study seeks to evaluate if the diagnostic performance of 18F-flurpiridaz positron emission tomography (PET) myocardial perfusion imaging (MPI), given the radiotracer's properties, is non-inferior to the currently most widely utilized PET MPI radiopharmaceutical, 82Rb-chloride.

Official Title

Comparative Evaluation of 18F-Flurpiridaz and 82Rb-Chloride PET Myocardial Perfusion Imaging: The FLARE (Flurpiridaz vs. Rubidium Evaluation) Trial

Details

  • Patients will undergo a clinically indicated rest/stress 82Rb-chloride positron emission tomography (PET) myocardial perfusion imaging (MPI) and will return to the nuclear cardiology laboratory within 1-30 days to undergo a 18F-flurpiridaz PET MPI and coronary CT angiogram. A rest 18F-flurpiridaz PET MPI will be acquired first, followed by a stress 18F-flurpiridaz PET MPI. The waiting period between the rest and stress 18F-flurpiridaz PET acquisitions will be ≥ 30 minutes. The rest dose will be 2.5-3.0 mCi, and the pharmacological stress dose will be 6.0-6.5 mCi. All PET MPI studies will be conducted using regadenoson as the pharmacologic stress agent.
  • 18F-flurpiridaz and 82Rb-chloride PET MPI scans will be interpreted by three expert visual readers in a blinded manner. Both Image quality and diagnostic certainty will be classified using a five-point scale. If the study is abnormal, the perfusion defect will further be categorized as reversible or fixed. Relative perfusion and myocardial blood flow quantification will be obtained using validated software methods.
  • Coronary CT angiograms will similarly be analyzed in a blinded manner by a core lab. Coronary segments with a diameter ≥1.5 mm will be included in the analysis. Each segment will be evaluated for the presence or absence of coronary atherosclerosis, defined as any tissue structure >1 mm2 within the coronary artery wall differentiated from the surrounding epicardial tissue, epicardial fat, or the vessel lumen itself. Maximal stenosis ratios as well as atherosclerotic plaque characteristics and CT-derived fractional flow reserve (FFR) will be obtained in each coronary territory.
  • The paired difference between 18F-flurpiridaz and 82Rb-chloride PET MPI will be evaluating by calculating the receiver operating characteristic area under the curve (ROC AUC) for the sensitivity and specificity of blinded visual reads, automated relative perfusion quantitation, and myocardial blood flow quantification, as well as for image quality and diagnostic certainty assessment.

Keywords

Coronary Artery Disease, Coronary Microvascular Disease, Myocardial Perfusion Imaging, Nuclear Cardiology, Positron Emission Tomography, Cardiac CT, Microvascular Angina

Eligibility

You can join if…

Open to people ages 18 years and up

  • Patient scheduled for a clinically indicated 82Rb-chloride PET MPI
  • Age ≥ 18 years
  • Ability to provide consent

You CAN'T join if...

  • Previous participation in a 18F-flurpiridaz clinical trial
  • Prior myocardial infarction
  • Prior coronary revascularization (percutaneous coronary intervention and/or coronary artery bypass grafting)
  • History of orthotopic heart transplantation
  • Inability to control heart rate < 65 bpm
  • Frequent ventricular or atrial ectopy leading to irregular cardiac rhythm
  • Creatinine ≥ 1.4 mg/dL
  • Pregnant or breast-feeding status

Location

  • West Los Angeles Veterans Affairs Medical Center
    Los Angeles California 90073 United States

Lead Scientist at UCLA

Details

Status
accepting new patients by invitation only
Start Date
Completion Date
(estimated)
Sponsor
University of California, Los Angeles
ID
NCT07761728
Study Type
Observational
Participants
Expecting 60 study participants
Last Updated