Magnetic Resonance Imaging (MRI) Viability: Comparison of Myocardial Viability by Positron Emission Tomography Versus MRI

This study is currently recruiting participants. (see Contacts and Locations)
Verified December 2013 by Emory University
Sponsor:
Information provided by:
Emory University
ClinicalTrials.gov Identifier:
NCT00166179
First received: September 13, 2005
Last updated: December 2, 2013
Last verified: December 2013

September 13, 2005
December 2, 2013
November 2003
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Complete list of historical versions of study NCT00166179 on ClinicalTrials.gov Archive Site
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Magnetic Resonance Imaging (MRI) Viability: Comparison of Myocardial Viability by Positron Emission Tomography Versus MRI
Comparison of Myocardial Viability by Positron Emission Tomography Versus Contrast-Enhanced Cardiac Magnetic Resonance Imaging

The purpose of this study is to compare cardiac MRI with positron emission tomography (PET) with fluorodeoxyglucose (FDG) to determine if cardiac MRI images are as good as, or better, than PET with FDG.

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Interventional
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Allocation: Non-Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Diagnostic
Coronary Artery Disease
Procedure: MRI
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
70
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Inclusion Criteria:

  • PET with FDG ordered

Exclusion Criteria:

  • Contraindicated for MRI
Both
18 Years to 95 Years
No
Contact: Rebecca Knoff, RN 404-686-1825 rebecca.knoff@emoryhealthcare.org
Contact: Kristen Moehring, RN 404-686-7289 kristen.moehring@emoryhealthcare.org
United States
 
NCT00166179
IRB00000292, 6-56550
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Emory University
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Principal Investigator: Randolph Patterson, MD Staff
Emory University
December 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP