Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 1:19 PM
Ignite Modification Date:
2025-12-24 @ 1:19 PM
NCT ID:
NCT00023595
Eligibility Criteria:
Inclusion Criteria:
* LV less than 35%, as defined by echocardiogram, left ventriculogram, CMR, or gated single photon emission computed tomography (SPECT) studies
* Coronary anatomy suitable for revascularization
Exclusion Criteria:
* Failure to provide informed consent.
* Aortic valvular heart disease clearly indicating the need for aortic valve repair or replacement.
* Cardiogenic shock (within 72 hours of randomization), as defined by the need for intraaortic balloon support or the requirement for intravenous inotropic support.
* Plan for percutaneous intervention of CAD.
* Recent acute MI judged to be an important cause of left ventricular dysfunction.
* History of more than 1 prior coronary bypass operation.
* Noncardiac illness with a life expectancy of less than 3 years.
* Noncardiac illness imposing substantial operative mortality.
* Conditions/circumstances likely to lead to poor treatment adherence (eg, history of poor compliance, alcohol or drug dependency, psychiatric illness, no fixed abode).
* Previous heart, kidney, liver, or lung transplantation.
* Current participation in another clinical trial in which a patient is taking an investigational drug or receiving an investigational medical device.
MED Therapy Eligibility Criteria
* Absence of left main CAD as defined by an intraluminal stenosis of 50% or greater.
* Absence of CCS III angina or greater (angina markedly limiting ordinary activity).
SVR Eligibility Criterion
• Dominant akinesia or dyskinesia of the anterior left ventricular wall amenable to SVR.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
100 Years
Study:
NCT00023595
Study Brief:
Protocol Section:
NCT00023595