Viewing Study NCT00286559



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Last Modification Date: 2024-10-26 @ 9:22 AM
Study NCT ID: NCT00286559
Status: WITHDRAWN
Last Update Posted: 2015-03-25
First Post: 2006-02-02

Brief Title: Assessing Myocardial Blood Flow and Blood Flow Reserve by Transoesophageal Echocardiography TEE
Sponsor: University Hospital Basel Switzerland
Organization: University Hospital Basel Switzerland

Study Overview

Official Title: Feasibility and Accuracy of Transoesophageal Harmonic Contrast Echocardiography in Assessing Myocardial Blood Flow and Blood Flow Reserve
Status: WITHDRAWN
Status Verified Date: 2015-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: echo contrast agents no longer allowed in CAD patients
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Until today it was not possible to reliably assess the function of a new bypass ie to measure myocardial perfusion Measuring intramyocardial blood flow directly after revascularisation would greatly improve the assessment of graft function With transthoracic contrast echocardiography myocardial perfusion can be reliably assessed as it has been shown in numerous studies In the first part of the study the investigators will clarify methodological aspects of contrast echocardiography In the second part they will analyze the validity of contrast TEE in the operating room
Detailed Description: Until today it was not possible to reliably assess the function of a new bypass ie to measure myocardial perfusion Measuring intramyocardial blood flow directly after revascularisation would greatly improve the assessment of graft function With transthoracic contrast echocardiography myocardial perfusion can be reliably assessed as it has been shown in numerous studies

As there is a new transoesophageal ultrasound probe on the market which allows contrast imaging we would like to establish contrast echocardiography in the operating room in patients undergoing CABG surgery

Ultrasound contrast agents eg SonoVue Optison consist of gas filled microspheres surrounded by a stabilizing coat They are smaller than red blood cells and similar to blood in their rheological habit The microspheres are injected into a peripheral or central vein They pass lung circulation and disperse into the left heart coronary arteries and body circulation A few minutes after administration the low-soluble gas of the microspheres is exhaled The interaction of the ultrasound beam with microspheres leads to oscillation of the microspheres and thereby amplification of the ultrasound signal This technique allows enhancement of endocardial border but also visualization of myocardial perfusion and assessment of myocardial blood flow reserve The latter requires measurement of myocardial perfusion a first time at rest and a second time during hyperemia with adenosine The quotient of both gives myocardial flow reserve This parameter is of paramount importance in cardiology to detect coronary artery stenosis and reduced coronary or myocardial flow reserve quantitatively

The contrast agents as well as adenosine a natural purine nucleoside which can be found in all cells of the body have a good safety profile with harmless and transient side effects Our patients will be under anesthesia and therefore feel none of those side effects

The study will be spread into two parts In a first part we will clarify methodological aspects of contrast echocardiography two different contrast agents and three different contrast imaging methods will be evaluated One imaging method and one contrast agent will be chosen for the second part In the second part we will analyze the validity of contrast TEE in the operating room In addition correlation of changes in myocardial blood flow after coronary artery bypass graft CABG surgery and improvement in myocardial perfusion as well as global and regional function in follow-up SPECT Single Photon Emission Computed Tomography and transthoracic echocardiography respectively will be evaluated By means of these data we possibly will be able to predict success of revascularisation at the end of surgery

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None