Magnetic Resonance Imaging (MRI) Viability: Comparison of Myocardial Viability by Positron Emission Tomography and MRI
2 other identifiers
observational
57
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Nov 2003
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 1, 2003
CompletedFirst Submitted
Initial submission to the registry
September 13, 2005
CompletedFirst Posted
Study publicly available on registry
September 14, 2005
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2006
CompletedStudy Completion
Last participant's last visit for all outcomes
October 1, 2006
CompletedSeptember 26, 2014
September 1, 2014
2.9 years
September 13, 2005
September 25, 2014
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Magnetic Resonance Imaging (MRI) Viability: Comparison of Myocardial Viability by Positron Emission Tomography and MRI
time of initial scans
Secondary Outcomes (1)
Compare size of regions of viable and non viable myocardium as % left ventricle by MRI vs. PET
at time of initial scans
Eligibility Criteria
Age \> 25 yrs, mean + SD = 60.3 + 10.2, 83% male, are patients referred by cardiologist or cardiac surgeon for assessment of myocardial viability by PET FDG.
You may qualify if:
- PET-FDG ordered to assess myocardial viability
You may not qualify if:
- Contraindicated for MRI
- Pregnant
- Age \<25 yrs
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Emory Universitylead
Study Sites (1)
Crawford Long Hospital
Atlanta, Georgia, 30308, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Randolph Patterson, MD
Staff
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
September 13, 2005
First Posted
September 14, 2005
Study Start
November 1, 2003
Primary Completion
October 1, 2006
Study Completion
October 1, 2006
Last Updated
September 26, 2014
Record last verified: 2014-09