Myocardial Perfusion Magnetic Resonance Imaging Using Regadenoson

Sponsor
Washington University School of Medicine (Other)
Overall Status
Completed
CT.gov ID
NCT00881218
Collaborator
Astellas Pharma US, Inc. (Industry)
50
1
1
30
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Study Details

Study Description

Brief Summary

This is a pilot study to determine whether the drug regadenoson can be used during magnetic resonance imaging to assess regions of poor blood flow to the heart.

The hypothesis of this study is that a single injection of regadenoson could be used instead of a standard adenosine infusion to produce coronary vasodilatation and demonstrate myocardial ischemia during first-pass perfusion cardiac MRI.

Condition or Disease Intervention/Treatment Phase
Early Phase 1

Detailed Description

This is a pilot study that proposes to assess the feasibility of using regadenoson (Lexiscan, Astellas), a recently FDA approved A2A receptor agonist, as the stress perfusion agent in cardiac MRI perfusion examinations. While regadenoson has been approved by the FDA, it has not been approved for the specific indications of use 1) during the simultaneous intravenous administration of a gadolinium-based contrast agent, or 2) during magnetic resonance imaging (MRI).

Because this agent can be given intravenously in a single 400 microgram bolus, rather than in an infusion, this agent may be easier to administer than adenosine during an MRI examination.

The objectives for this pilot study are: 1) To demonstrate the feasibility of using regadenoson during cardiac perfusion MRI to visualize known regions of myocardial ischemia as demonstrated on SPECT-MPI and 2) To describe a cardiac perfusion MRI protocol using regadenoson that would have the potential to be used clinically.

Study Design

Study Type:
Interventional
Actual Enrollment :
50 participants
Allocation:
Non-Randomized
Intervention Model:
Single Group Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Diagnostic
Official Title:
Feasibility of Detecting Myocardial Ischemia by First-pass Contrast MRI Using Regadenoson
Study Start Date :
Jun 1, 2009
Actual Primary Completion Date :
Dec 1, 2011
Actual Study Completion Date :
Dec 1, 2011

Arms and Interventions

Arm Intervention/Treatment
Experimental: Regadenoson CMR

Images in the cardiac short axis will be obtained using a gradient recalled echo sequence, TR 2.3 msec/TE 1.1 msec, 80*256 matrix, slice thickness 10 mm. Images will be obtained during power injection of 0.075 mmol/Kg of a conventional gadolinium based MR contrast agent at a rate of 5 mL/sec followed by a 15 mL saline flush into an antecubital vein. Perfusion imaging will be performed at stress and rest. Stress: Regadenoson 400 mcg will be administered IV bolus via an antecubital cannula. Immediately after injection, MR scanning will begin and contrast will be given. Rest: After 10 minutes, rest imaging will be performed identically, but without regadenoson injection. To identify late enhancement of myocardial tissue inversion recovery prepared images will be obtained.

Drug: Regadenoson
Regadenoson 400 micrograms will be administered IV bolus via an antecubital cannula.
Other Names:
  • Lexiscan
  • Outcome Measures

    Primary Outcome Measures

    1. Feasibility of use of regadenoson during cardiac perfusion MRI to visualize regions of myocardial ischemia as demonstrated on SPECT-MPI. [1 year]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • reversible perfusion abnormalities on a clinically ordered rest/adenosine dual-isotope SPECT-MPI in at least 2 contiguous myocardial segments (per 17-segment model)
    Exclusion Criteria:
    • myocardial infarction, myocardial revascularization procedure or progression in angina occuring after the SPECT-MPI examination

    • pregnancy

    • gadolinium-based MR contrast allergy

    • glomerular filtration rate (GFR) > 60 mL/min/1.73 m2

    • contraindications to MR imaging (pacemaker, brain aneurysm clips, schrapnel, etc.)

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Washington University School of Medicine St. Louis Missouri United States 63110

    Sponsors and Collaborators

    • Washington University School of Medicine
    • Astellas Pharma US, Inc.

    Investigators

    • Principal Investigator: Pamela K. Woodard, M.D., Washington University School of Medicine

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Pamela Woodard, MD, M.D., FACR, FAHA, FCCP, Washington University School of Medicine
    ClinicalTrials.gov Identifier:
    NCT00881218
    Other Study ID Numbers:
    • REGADENOSON.MRI.WUSTL
    First Posted:
    Apr 15, 2009
    Last Update Posted:
    Apr 10, 2012
    Last Verified:
    Apr 1, 2012
    Keywords provided by Pamela Woodard, MD, M.D., FACR, FAHA, FCCP, Washington University School of Medicine
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 10, 2012