Status:

COMPLETED

Cadmium-zinc-telluride (CZT) Imaging of Myocardial Blood Flow (MBF) (SPECT MBF)

Lead Sponsor:

Ottawa Heart Institute Research Corporation

Collaborating Sponsors:

GE Healthcare

Conditions:

Coronary Heart Disease

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

This study is being done to compare the blood flow measurements obtained with the SPECT and PET imaging scans. Measurements such as myocardial blood flow (MBF) and myocardial flow reserve (MFR) are an...

Detailed Description

Absolute myocardial blood flow (MBF) and myocardial flow reserve (MFR) are calculated measurements that are obtained using positron emission tomography (PET) nuclear imaging, from a myocardial perfusi...

Eligibility Criteria

Inclusion

  • For all participants
  • Age ≥ 18 years old
  • BMI ≤ 40 kg/m2
  • Able and willing to comply with the study procedures
  • Written informed consent Participants with intermediate to high probability of CAD
  • Suspected or known CAD on a stable medication regime. Healthy volunteers without known heart disease
  • Low risk of CAD (ACC Guidelines Pre-test Probability of Coronary Disease by Symptoms, Gender and Age)

Exclusion

  • History or risk of severe bradycardia (heart rate \< 50 beats per minute) not related to chronotropic drugs
  • Known second- or third-degree AV block without pacemaker
  • Dyspnea (NYHA III/IV), wheezing asthma or COPD
  • Coronary artery bypass graft (CABG) surgery within 60 days prior to screening or at any time after consent
  • Percutaneous coronary intervention (PCI) within 30 days prior to screening or at any time following consent
  • Acute myocardial infarction or acute coronary syndrome within 60 days prior to screening or at any time following consent
  • Recent use of dipyridamole, dipyridamole-containing medications (e.g. Aggrenox)
  • Known hypersensitivity to dipyridamole
  • Breastfeeding or pregnancy
  • Claustrophobia or inability to lie still in a supine position
  • Unwillingness or inability to provide informed consent

Key Trial Info

Start Date :

October 30 2014

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

September 2 2022

Estimated Enrollment :

66 Patients enrolled

Trial Details

Trial ID

NCT02280941

Start Date

October 30 2014

End Date

September 2 2022

Last Update

April 6 2025

Active Locations (1)

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1

University of Ottawa Heart Institute

Ottawa, Ontario, Canada, K1Y 4W7