Trials / Terminated
TerminatedNCT02062008
Validation of Combined PET-MR Quantitative Parameters for Cardiac Applications
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 2 (actual)
- Sponsor
- University of California, San Francisco · Academic / Other
- Sex
- All
- Age
- 18 Years – 90 Years
- Healthy volunteers
- Not accepted
Summary
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.
Detailed 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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | PET-MRI | PET-MRI with intravenous Gadolinium and FDG. The entire study will take approximately one hour. |
Timeline
- Start date
- 2016-12-01
- Primary completion
- 2018-02-10
- Completion
- 2018-02-10
- First posted
- 2014-02-13
- Last updated
- 2021-06-16
- Results posted
- 2021-06-16
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT02062008. Inclusion in this directory is not an endorsement.