About this trial
Cardiac allograft vasculopathy (CAV) is a common complication affecting heart transplant patients. This condition causes narrowing of the heart arteries leading to graft dysfunction. Surveillance for CAV is vital; however an ideal approach has not been established. The goal of this study is to assess whether noninvasive positron emission tomography (PET) based surveillance is non-inferior to invasive coronary angiography (ICA) surveillance.
Eligibility criteria
Qualifiers
Post heart transplant 2-10 years.
Age ≥18 years.
Able to provide informed consent.
Disqualifiers
Contraindication to dipyridamole due to severe aortic stenosis.
Contraindication to dipyridamole due to 2:1 or greater AV block without pacemaker.
Contraindication to dipyridamole due to severe bronchospasm.
Unable to undergo coronary angiography due to allergy to iodinated contrast.
Trial design
Treatments tested in this trial
- ICA
- PET
Treatment groups
Sponsors and collaborators
Ottawa Heart Institute Research Corporation
Lead sponsor
Canadian Institutes of Health Research (CIHR)
Collaborator