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Quantitative 13N-Ammonia Cardiac Rest/Stress Digital PET/CT

Stanford University logo

Stanford University

Status

Completed

Conditions

Coronary Artery Disease

Treatments

Drug: Regadenoson
Diagnostic Test: Cardiac Perfusion Rest/Stress Digital PET/CT
Drug: N-13 ammonia

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT03170817
IRB 39331

Details and patient eligibility

About

Accurate measurements from a non-invasive test like myocardial perfusion positron emission tomography/ computed tomography (PET/CT) may decrease the need for invasive procedures such as cardiac catheterization.The investigators wish to see if the measurements from cardiac catheterization can be predicted using a non-invasive 13N-NH3 digital PET/CT scan.

Full description

Cardiac imaging using standard-of-care Nuclear Medicine techniques assess the relative radiopharmaceutical distribution from coronary arteries to cardiac tissue. This standard interpretation however, lacks the clinical utility of modern quantitative techniques that are now routinely obtained during cardiac catheterization, such as fractional flow reserve (FFR). Cardiologists routinely base critical management decisions, including the choice for revascularization, stenting, or angioplasty, on these measurements.

Non-invasive measurements of MBF (Myocardial Blood Flow), CFR (Coronary Flow Reserve) and RFR (Relative Flow Reserve) using PET/CT have been investigated, but have yet to reach clinicl use. Given the inherent gains in sensitivity and resolution, digital PET/CT, may allow for a more robust and accurate platform to obtain quantitative measurements of MBF, CFR and RFR which may greatly enhance the clinical utility of cardiac PET/CT for management of coronary artery disease.

Enrollment

15 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient is ≥ 18 years old at the time of the scan
  • Patient has known or suspected coronary artery disease
  • Patient has had a recent or will be scheduled for a diagnostic coronary angiogram
  • Patient provides written informed consent
  • Patient is referred for myocardial perfusion scan
  • Patient is capable of complying with study procedures
  • Patient is able to remain still for duration of imaging procedure (approximately 60 minutes total for both PET/CT)

Exclusion criteria

  • Patients who are pregnant or breast feeding
  • Patients with contraindications to regadenoson

Trial design

15 participants in 1 patient group

N13-ammonia Cardiac Rest/Stress PET/CT
Description:
Patients with coronary artery disease (CAD) undergo a Cardiac Perfusion Rest/Stress Digital PET/CT scan using the radiopharmaceutical N13-ammonia and Regadenoson (Lexiscan) to induce pharmacologic stress.
Treatment:
Drug: N-13 ammonia
Drug: Regadenoson
Diagnostic Test: Cardiac Perfusion Rest/Stress Digital PET/CT

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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