PET MRI in Coronary Artery Disease

University of Edinburgh

Status: Completed

Conditions: Coronary Artery Disease

Treatments: Diagnostic Test: PET/MRI; Diagnostic Test: MRI

Study type: Observational

Funder types: Other

Identifiers

NCT03451448

17/SS/0151

Details and patient eligibility

About

This study will assess the use of position emission tomography/magnetic resonance imaging (PET/MRI) using ultra-small-superparamagnetic particles of iron oxide (USPIO) as a contrast agent in patients with coronary artery disease.

Full description

Positron emission tomography/magnetic resonance imaging (PET/MRI) has the potential to provide detailed information on coronary artery anatomy, the presence of coronary artery stenosis, the composition of atherosclerotic plaque using MRI tissue characterisation and information about the underlying biological processes using targeted PET tracers. Ultra-small-superparamagnetic particles of iron oxide (USPIO) have a long blood pool half-life so are an ideal contrast agent for PET/MRI imaging.

This study will assess the use of PET/MRI with USPIO in patients with stable coronary artery disease and recent acute myocardial infarction.

Enrollment: 16 patients

Sex: All

Ages: 40+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Healthy volunteers to undergo MRI imaging will be over the age of 18 years and able to provide informed consent.
• Patients with coronary artery disease to undergo PET/MRI will have multi-vessel disease (≥2 vessel coronary artery disease with ≥ 50% cross-sectional luminal stenosis).
• able to provide informed consent
• over the age of 40 years

Exclusion criteria

• inability or unwillingness to undergo magnetic resonance imaging or positron emission tomography
• renal failure (Serum creatinine >200 umol/L or estimated glomerular filtration rate <30 mL/min
• hepatic failure
• pregnancy
• inability to provide informed consent
• contraindications to undergoing MRI scanning
• contraindications to contrast agents not included above including evidence of iron overload, known allergy to constituents of the contrast agents, and anaemia not caused by iron deficiency

Trial design

16 participants in 3 patient groups

Healthy volunteers

Description:

Healthy volunteers to undergo MRI using USPIO contrast

Treatment:

Diagnostic Test: MRI

Stable coronary artery disease

Description:

Patients with coronary artery disease without recent (3 months) acute coronary syndrome or revascularisation

Treatment:

Diagnostic Test: PET/MRI

Recent acute coronary syndrome

Description:

Patients with recent (3 months) type 1 myocardial infarction

Treatment:

Diagnostic Test: PET/MRI