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

Sponsor
Stanford University (Other)
Overall Status
Completed
CT.gov ID
NCT03170817
Collaborator
GE Healthcare (Industry)
15
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53.1
0.3

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Cardiac Perfusion Rest/Stress Digital PET/CT
  • Drug: N-13 ammonia
  • Drug: Regadenoson

Detailed 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.

Study Design

Study Type:
Observational
Actual Enrollment :
15 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Quantitative Rest/Stress Cardiac Perfusion Digital PET/CT: Comparison Between Noninvasive Imaging and Invasive Coronary Angiography.
Actual Study Start Date :
Mar 29, 2017
Actual Primary Completion Date :
Mar 31, 2020
Actual Study Completion Date :
Sep 1, 2021

Arms and Interventions

Arm Intervention/Treatment
N13-ammonia Cardiac Rest/Stress PET/CT

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.

Diagnostic Test: Cardiac Perfusion Rest/Stress Digital PET/CT
Patients with coronary artery disease undergo a N-13 ammonia rest/stress PET/CT scan. These patients are given: One 5-10 mCI N13-ammonia (13N-NH3) intravenously and undergo a rest digital PET/CT scan of ~20 minute duration. A dose of 0.4 mg regadenoson (Lexiscan) intravenously over 10 seconds to increase blood flow to the heart One 5-10 mCi N13-ammonia (13N-NH3) intravenously and undergo a stress digital PET/CT scan of ~20 minute duration Total patient time will take approximately up to 120 minutes.

Drug: N-13 ammonia
5-10 mCi intravenous injection of N-13 ammonia radiopharmaceutical at rest and at stress

Drug: Regadenoson
0.4 mg/5mL intravenous injection to induce pharmacologic stress (Astellas Pharma US, Inc.)
Other Names:
  • Lexiscan
  • Outcome Measures

    Primary Outcome Measures

    1. MBF measurement using PET/CT [an estimated average of 2 hours]

      Non-invasive measurements of myocardial blood flow (MBF) in milliliter/minute/gram using PET/CT scanner will be compared to invasive cardiac angiography values (current gold standard). MBF values are obtained using image-derived time activity curves from the left ventricular blood and myocardial tissue regions. These values represent radiotracer exchange between the blood and the tissue over time. The rate of radiotracer uptake into the myocardial tissue provides an estimate of MBF. Processing software will then use the time-activity curves to calculate MBF at rest and at stress.

    2. CFR measurement using PET/CT [an estimated average of 2 hours]

      Non-invasive measurements of coronary flow reserve (CFR) using digital PET/CT scanner will be compared to the gold standard evaluation from invasive cardiac angiography. Discrepancy between PET measurements and cardiac angiography results will be reported. CFR is the ratio of MBF at peak blood flow to resting MBF.

    3. RFR measurement using PET/CT [an estimated average of 2 hours]

      Non-invasive measurements of relative flow reserve (RFR) using digital PET/CT scanner will be compared to the gold standard evaluation from invasive cardiac angiography. Discrepancy between PET measurements and cardiac angiography results will be reported. RFR is the ratio of MBF during stress in an affected region of the left ventricle (LV) to MBF during stress in a normal region of the LV.

    Secondary Outcome Measures

    1. NM Physician diagnostic confidence of 13N-NH3 PET/CT [an estimated average of 2 hours]

      Nuclear medicine physician diagnostic confidence will be assessed using a 5-point Likert scale. NM Physicians will compare images obtained from the 13N-NH3 PET/CT to images obtained from single photon emission computed tomography/CT (SPECT/CT).

    2. Overall Exam Time [an estimated average of 2 hours]

      Overall study time as counted from initial administration of radiopharmaceutical to completion of image acquisition will be measured and compared to SPECT/CT overall exam time.

    3. Effective radiation dose [an estimated average of 2 hours]

      Total radiation dose (measured in mSv) from 13N-NH3 PET/CT will be measured and compared to the dose typically given to patients during standard myocardial perfusion imaging SPECT/CT studies.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    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

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Stanford University Stanford California United States 94305

    Sponsors and Collaborators

    • Stanford University
    • GE Healthcare

    Investigators

    • Principal Investigator: Guido Davidzon, MD, MS, Stanford University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Guido A. Davidzon, MD, SM, Clinical Assistant Professor, Stanford University
    ClinicalTrials.gov Identifier:
    NCT03170817
    Other Study ID Numbers:
    • IRB 39331
    First Posted:
    May 31, 2017
    Last Update Posted:
    Oct 26, 2021
    Last Verified:
    Oct 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    Yes
    Product Manufactured in and Exported from the U.S.:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 26, 2021