NCT00417625

Brief Summary

This study will test the accuracy of magnetic resonance imaging (MRI) in measuring cardiac perfusion (blood flow). MRI of the heart can measure blood flow to heart muscle, but collateral coronary arteries (vessels that supply blood to the heart muscle) may reduce the accuracy of the measurements. This study will perform special measurements of coronary artery flow and pressure in patients undergoing heart catheterization and catheter-based treatment (angioplasty and stenting) in order to compare for accuracy with cardiac MRI. Patients 21 years of age and older with coronary artery blockage may be eligible for this study. All participants undergo cardiac MRI, to produce images of the heart, as well as special invasive blood flow testing during heart catheterization, angioplasty, and stenting. During MRI, the subject lies on a table that can slide in and out of the scanner (a narrow cylinder), wearing earplugs to muffle loud knocking and thumping sounds that occur during the scanning process. The procedure lasts about 45 to 90 minutes. Since the heart moves during breathing, subjects are asked to hold their breath intermittently for about 5-20 seconds. A medicine called dipyridamole is injected through a vein in the subject's arm to increase blood flow to the coronary arteries and help detect blockages. Pictures are taken of the heart before, during, and after the dipyridamole injection. Another medicine called gadolinium is also given through a vein. This medicine brightens the images to measure blood flow. During a separate catheterization, angioplasty, and stenting procedure, subjects undergo additional invasive tests. The additional tests use a special guidewire to measure coronary artery pressure and blood flow, as well as a special ultrasound to look inside the artery. Patients have a repeat MRI about 2 months after the catheterization.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
34

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Dec 2006

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

December 29, 2006

Completed
1 day until next milestone

First Submitted

Initial submission to the registry

December 30, 2006

Completed
5 days until next milestone

First Posted

Study publicly available on registry

January 4, 2007

Completed
3.5 years until next milestone

Study Completion

Last participant's last visit for all outcomes

July 19, 2010

Completed
Last Updated

July 2, 2017

Status Verified

July 19, 2010

First QC Date

December 30, 2006

Last Update Submit

June 30, 2017

Conditions

Keywords

Coronary Artery PerfusionMRIFractional Flow ReserveCoronary Flow ReserveCollateral Artery PerfusionCardiovascular DiseaseCoronary Artery DiseaseCAD

Eligibility Criteria

Age21 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Patients with known or suspected cardiovascular disease
  • Age above age 21 (coronary artery disease is rare in subjects less than age 21)
  • Undergoing medically necessary coronary arteriography
  • Written informed consent
  • The subject must allow access to the use of previous medical information from NIH or any institution in order to participate in the research study.

You may not qualify if:

  • Pregnant women (when uncertain, subjects will undergo urine or blood testing) or lactating women
  • Decompensated congestive heart failure (unable to lie flat during MRI or catheterization)
  • Impaired renal excretory function (calculated Glomerular Filtration Rate less than 30mL/min/1.73m(2)) unless on dialysis.
  • Cardiac pacemaker or implantable defibrillator
  • Cerebral aneurysm clip
  • Neural stimulator (e.g. TENS-Unit)
  • Any type of ear implant
  • Ocular foreign body (e.g. metal shavings)
  • Any implanted device (e.g. insulin pump, drug infusion device)
  • Metal shrapnel or bullet.
  • Unable to tolerate dipyridamole:
  • Reactive airways disease (significant asthma or chronic obstructive pulmonary disease and unable to tolerate a beta adrenergic antagonist).
  • Excessive tortuosity or any angiographic features that, in the opinion of catheterization operator, would make invasive physiology assessments unsafe or unsuitable
  • Ongoing myocardial ischemia or other exigency that would make further study participation hazardous
  • Normal epicardial coronary arteries and normal perfusion cardiac MRI

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

National Institutes of Health Clinical Center, 9000 Rockville Pike

Bethesda, Maryland, 20892, United States

Location

Related Publications (3)

  • Muehling OM, Jerosch-Herold M, Panse P, Zenovich A, Wilson BV, Wilson RF, Wilke N. Regional heterogeneity of myocardial perfusion in healthy human myocardium: assessment with magnetic resonance perfusion imaging. J Cardiovasc Magn Reson. 2004;6(2):499-507. doi: 10.1081/jcmr-120030570.

    PMID: 15137334BACKGROUND
  • Jerosch-Herold M, Swingen C, Seethamraju RT. Myocardial blood flow quantification with MRI by model-independent deconvolution. Med Phys. 2002 May;29(5):886-97. doi: 10.1118/1.1473135.

    PMID: 12033585BACKGROUND
  • Muhling OM, Dickson ME, Zenovich A, Huang Y, Wilson BV, Wilson RF, Anand IS, Seethamraju RT, Jerosch-Herold M, Wilke NM. Quantitative magnetic resonance first-pass perfusion analysis: inter- and intraobserver agreement. J Cardiovasc Magn Reson. 2001;3(3):247-56. doi: 10.1081/jcmr-100107473.

    PMID: 11816621BACKGROUND

MeSH Terms

Conditions

Coronary Artery DiseaseCardiovascular Diseases

Condition Hierarchy (Ancestors)

Coronary DiseaseMyocardial IschemiaHeart DiseasesArteriosclerosisArterial Occlusive DiseasesVascular Diseases

Study Design

Study Type
observational
Time Perspective
PROSPECTIVE
Sponsor Type
NIH

Study Record Dates

First Submitted

December 30, 2006

First Posted

January 4, 2007

Study Start

December 29, 2006

Study Completion

July 19, 2010

Last Updated

July 2, 2017

Record last verified: 2010-07-19

Locations