Comparison of Echocardiographic Techniques in Diagnosis of Coronary Artery Disease

Sponsor
National Heart, Lung, and Blood Institute (NHLBI) (NIH)
Overall Status
Completed
CT.gov ID
NCT00001889
Collaborator
(none)
150
1
24
6.2

Study Details

Study Description

Brief Summary

This study is designed to compare two different echocardiographic techniques in the evaluation of heart disease (coronary artery disease). Both tests called Myocardial Contrast Echocardiography with Pharmacologic Stress and Stress Echocardiography with Dobutamine, are performed using a standard echocardiographic machine.

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. It is important to observe the heart during exercise because there are changes in blood flow. Since MCE cannot be performed when the patient is exercising, researchers give medication (adenosine) that stimulates the heart and creates a situation similar to exercise.

Stress 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.

The purpose of this study is to evaluate the accuracy of MCE compared to stress echocardiography at detecting coronary artery disease (CAD).

Condition or Disease Intervention/Treatment Phase
  • Procedure: Myocardial contrast echocardiography
  • Procedure: Stress echocardiography with dobutamine
Phase 2

Detailed Description

Stress echocardiography has become a valuable technique for the non-invasive detection of coronary artery disease (CAD). Its accuracy has been shown to be superior to that of the exercise electrocardiogram and comparable to that of myocardial perfusion imaging. Myocardial contrast echocardiography (MCE) offers the potential to evaluate tissue perfusion at the level where oxygen transfer to the myocytes occurs. MCE can, therefore, provide information regarding the functional status of the myocardial microvasculature and presence of blood flow disparity. The purpose of this study is to evaluate the accuracy of MCE compared to stress echocardiography. We will correlate these results with findings from coronary angiography and compare the ability of those techniques to detect CAD.

Study Design

Study Type:
Interventional
Primary Purpose:
Treatment
Official Title:
Comparison of Myocardial Contrast Echo With Dobutamine Echo in Diagnosis of Coronary Artery Disease
Study Start Date :
Mar 1, 1999
Study Completion Date :
Mar 1, 2001

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No

    Patients with known or suspected coronary artery disease.

    Adults 18 years of age or older.

    No pre-menopausal patients who are lactating, pregnant or potentially pregnant as judged by history, physical examination, ultrasound or urine pregnancy test.

    No unstable angina patients.

    No recent myocardial infarction patients (less than 1 month).

    No frequent ectopy which precludes adequate image acquisition.

    No history of asthma or chronic obstructive pulmonary disease.

    No patients receiving aminophylline, theophylline or dipyridamole.

    No presence of second and third degree heart block without pacemaker.

    No significant hypertension (systolic blood pressure greater than 170 mm Hg) or hypotension (systolic blood pressure less than 100 mm Hg).

    No hypotension: basal sitting systolic arterial pressure less than 100 mm Hg confirmed 30 minutes later.

    No sinus tachycardia greater than or equal to 100 beats per min.

    No atrial fibrillation.

    No inadequate two-dimensional echocardiographic windows.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 National Heart, Lung and Blood Institute (NHLBI) Bethesda Maryland United States 20892

    Sponsors and Collaborators

    • National Heart, Lung, and Blood Institute (NHLBI)

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00001889
    Other Study ID Numbers:
    • 990077
    • 99-H-0077
    First Posted:
    Dec 10, 2002
    Last Update Posted:
    Mar 4, 2008
    Last Verified:
    Feb 1, 2000

    Study Results

    No Results Posted as of Mar 4, 2008