Myocardial Contrast Echocardiography (MCE) to Check for Living and Working Heart Muscle
NCT ID: NCT00001891
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
PHASE3
200 participants
INTERVENTIONAL
1999-05-31
2001-03-31
Brief Summary
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The purpose of this study is to compare the accuracy of myocardial contrast echocardiography (MCE) to dobutamine echocardiography to detect the potential for damaged heart muscle to be treated and function in patients with heart disease.
Myocardial contrast echocardiography (MCE) does not use radioactivity. It uses sound waves like standard echocardiography. However, with MCE patients receive an injection of a "contrast agent" directly into the blood stream through a vein. The contrast agent, called Optison, is made of tiny microbubbles smaller than red blood cells. The echocardiogram can detect these microbubbles in the small blood vessels of the heart muscle and allow researchers to find areas of the heart receiving less blood flow than others.
Echocardiography with Dobutamine does not use radioactivity. It uses sound waves, like standard echocardiography. During this echocardiogram patients receive doses of a medication called dobutamine that stimulates the heart to beat stronger and faster. Heart muscle that does not beat stronger after dobutamine is probably dead, usually as a result of a previous heart attack.
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Detailed Description
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Conditions
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Study Design
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TREATMENT
Interventions
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Myocardial contrast echocardiography
Dobutamine echocardiography
Eligibility Criteria
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Inclusion Criteria
Patients will be adults older than 21 years of age.
No pre-menopausal patients who are lactating, are pregnant or potentially pregnant as judged by history, physical examination, ultrasound or urine pregnancy test.
No one with unstable angina.
No subjects with recent myocardial infarction (less than 1 month).
No one with frequent ectopy which precludes adequate imaging acquisition.
No subjects with significant hypertension (systolic blood pressure greater than 170 mm Hg).
No hypotension with basal sitting systolic arterial pressure less than 100 mm HG confirmed 30 minutes later.
No subjects with sinus tachycardia greater than or equal to 100 beats/minute.
No atrial fibrillation.
No inadequate two-dimensional echocardiographic windows.
ALL
No
Sponsors
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National Heart, Lung, and Blood Institute (NHLBI)
NIH
Locations
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National Heart, Lung and Blood Institute (NHLBI)
Bethesda, Maryland, United States
Countries
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References
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Maisey M. Evaluating the benefits of nuclear cardiology. Q J Nucl Med. 1996 Mar;40(1):47-54.
Vanoverschelde JL, Wijns W, Depre C, Essamri B, Heyndrickx GR, Borgers M, Bol A, Melin JA. Mechanisms of chronic regional postischemic dysfunction in humans. New insights from the study of noninfarcted collateral-dependent myocardium. Circulation. 1993 May;87(5):1513-23. doi: 10.1161/01.cir.87.5.1513.
Other Identifiers
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99-H-0108
Identifier Type: -
Identifier Source: secondary_id
990108
Identifier Type: -
Identifier Source: org_study_id
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