NCT00166179

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
57

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Nov 2003

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 1, 2003

Completed
1.9 years until next milestone

First Submitted

Initial submission to the registry

September 13, 2005

Completed
1 day until next milestone

First Posted

Study publicly available on registry

September 14, 2005

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2006

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2006

Completed
Last Updated

September 26, 2014

Status Verified

September 1, 2014

Enrollment Period

2.9 years

First QC Date

September 13, 2005

Last Update Submit

September 25, 2014

Conditions

Keywords

CAD

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

Age18 Years - 95 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

Study Sites (1)

Crawford Long Hospital

Atlanta, Georgia, 30308, United States

Location

MeSH Terms

Conditions

Coronary Artery Disease

Condition Hierarchy (Ancestors)

Coronary DiseaseMyocardial IschemiaHeart DiseasesCardiovascular DiseasesArteriosclerosisArterial Occlusive DiseasesVascular Diseases

Study Officials

  • Randolph Patterson, MD

    Staff

    PRINCIPAL INVESTIGATOR

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

Locations