Magnetic Resonance Angiography (MRA) for the Diagnosis of Atherosclerosis
NCT ID: NCT00001841
Last Updated: 2008-03-04
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
100 participants
OBSERVATIONAL
1999-03-31
2004-12-31
Brief Summary
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The purpose of this study is to recruit patients diagnosed with or suspected of having, atherosclerosis (hardening of the arteries) to participate in a series of new state-of-the-art diagnostic tests using MRA.
This study is a combined effort between the National Institutes of Health (NIH), Uniformed Services University of the Health Sciences (USUHS), and General Electric Medical Services and is supported a Cooperative Research Agreement is to (CRADA).
The goal of this study is to improve MRA to the point that it can reliably replace diagnostic x-ray catheter angiography in the evaluation of patients with atherosclerosis.
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Detailed Description
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Conditions
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Eligibility Criteria
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Inclusion Criteria
Patients must have suspected atherosclerotic disease based on clinical findings or documented by angiography or doppler ultrasound performed within 3 months of the MRA.
Patients must be willing to participate in the protocol.
Patients must be referred by a physician who is caring for the patient and to whom the results will be provided.
Patients must be clinically stable and be judged by their physician able to come to the Clinical Center to participate in the study.
Patients must have serum Creatinine value less than 3.0 mg/dl.
Exclusion Criteria
(a) pacemaker or other implanted electronic device; (b) cochlear implants; (c) metal in the eye; (d) embedded shrapnel fragments; (e) cerebral aneurysm clips; or (f) medical infusion pumps.
Allergy to Gadolinium based contrast media.
Unsatisfactory performance status as judged by the referring physician such that the patient could not tolerate an MRI scan. Examples of medical conditions that would not be accepted would include angina, dyspnea at rest, congestive heart failure, severe claudication (less than 1 flight of steps).
Intercurrent illness that requires treatment that would be jeopardized by the MRA scan.
Subjects requiring sedation for MRI studies.
Pregnant female.
Patients with severe back-pain who will be unable to tolerate supine positioning within the MRI scanner for the duration of the examination.
ALL
No
Sponsors
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National Institutes of Health Clinical Center (CC)
NIH
Locations
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Warren G. Magnuson Clinical Center (CC)
Bethesda, Maryland, United States
Countries
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References
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Prince MR, Yucel EK, Kaufman JA, Harrison DC, Geller SC. Dynamic gadolinium-enhanced three-dimensional abdominal MR arteriography. J Magn Reson Imaging. 1993 Nov-Dec;3(6):877-81. doi: 10.1002/jmri.1880030614.
Prince MR. Peripheral vascular MR angiography: the time has come. Radiology. 1998 Mar;206(3):592-3. doi: 10.1148/radiology.206.3.9494471. No abstract available.
Prince MR. Contrast-enhanced MR angiography: theory and optimization. Magn Reson Imaging Clin N Am. 1998 May;6(2):257-67.
Other Identifiers
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99-CC-0061
Identifier Type: -
Identifier Source: secondary_id
990061
Identifier Type: -
Identifier Source: org_study_id
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