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Validation of Combined PET-MR Quantitative Parameters for Cardiac Applications

University of California San Francisco (UCSF) logo

University of California San Francisco (UCSF)

Status

Terminated

Conditions

Cardiac Disease

Treatments

Device: PET-MRI

Study type

Interventional

Funder types

Other

Identifiers

NCT02062008
Combined PET-MRI

Details and patient eligibility

About

The purpose of this study is to understand how simultaneous PET/MR acquisition can provide novel qualitative and quantitative biomarkers to guide clinical intervention and predict prognosis of patients with cardiovascular disease.

Full description

  • To compare regional myocardial uptake of FDG on images obtained on a standard PET camera with the new PET/MR camera, in patients with coronary artery disease.
  • To compare viability maps obtained with cardiac MR images and FDG-PET for delineation of myocardial infarct core and border zone, in patients with coronary artery disease.
  • To correlate MRI myocardial strain with relative myocardial FDG uptake in patients with a previous myocardial infarction.
  • To interrogate if simultaneous acquisition of cardiac PET and viability cardiac MR differ from acquisitions obtained independently, with special focus on attenuation correction methods
  • To combined MRI scar map with FDG-PET uptake in patients with cardiac sarcoidosis and myocarditis.
  • To correlate morphologic characteristics of atherosclerotic disease in the thoracic and abdominal aorta with FDG uptake and ferumoxytol enhancement, as a marker of inflammation.
  • To evaluate cardiac strain and myocardial scar burden in obese patients with and without diabetes.

Enrollment

2 patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Subjects with ischemic and non-ischemic cardiac disease referred for cardiac PET for viability imaging.

Exclusion criteria

  • Contraindications for MRI, including cardiac pacemaker, claustrophobia, retained metallic foreign body, cochlear implant, Aneurysm clip in the brain, pregnancy and eGFR less than 45%.

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

2 participants in 1 patient group

Cardiac patients receiving PET/MR
Other group
Description:
PET-MRI with intravenous Gadolinium and FDG. The entire study will take approximately one hour.
Treatment:
Device: PET-MRI

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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