Cell Therapy in Chronic Ischemic Heart Disease

Ministry of Health, Brazil

Status and phase

Terminated

Phase 3

Conditions

Coronary Artery Disease

Ischemic Heart Disease

Treatments

Procedure: Intramyocardial injection of autologous bone marrow cells

Study type

Interventional

Funder types

Other

Identifiers

NCT00362388

EMRTCC-ISQ

Details and patient eligibility

About

This study was designed to test the hypothesis that direct injection of bone-marrow cells in the heart may increase the number of blood vessels, ameliorating the heart's performance, and relieving patients from symptoms like angina and/or shortness of breath.

Full description

Severe ischemic heart disease (IHD) remains a clinical challenge; many patients with IHD have undergone myocardial revascularization procedures (either percutaneous or surgical) but still remain symptomatic despite maximally tolerated medical therapy. Others are considered non-optimal candidates for a complete myocardial revascularization procedure due to the extension and diffuseness of the disease.

Cell therapy with autologous bone marrow-derived cells (BMC) is a novel therapeutic strategy being tested for many cardiovascular diseases, including heart failure, acute myocardial infarction, chronic ischemic heart disease.

The primary objective of this study is to assess the efficacy of intramyocardial injection of autologous BMC on the myocardial perfusion and left ventricular function as an adjunctive therapy (compared to placebo) in patients undergoing coronary artery bypass surgery (CABG).

The secondary objective of this study is to assess the effect of intramyocardial injection of autologous BMC on functional class (angina/heart failure), functional capacity, global and cardiovascular mortality, and quality of life in patients undergoing coronary artery bypass surgery (CABG).

Enrollment

300 estimated patients

Sex

All

Ages

30 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Diagnosis of chronic, severe, diffuse, multivessel atherosclerotic coronary artery disease (CAD) referred for CABG.
Echocardiogram-assessed LVEF between 25 and 55% (Simpson's rule).
Angina (or equivalent) functional class II to IV (Canadian Cardiovascular Society) despite maximally tolerated medical therapy.
Abnormal myocardial perfusion tests:

i. Cardiac scintigraphy ii. Magnetic resonance imaging iii. Dobutamine-atropine stress-echocardiogram
Non-candidates for a percutaneous coronary intervention (PCI) due to ANY of the following:

i. High risk lesion ii. Extensive lesion iii. Diffuse, small vessel disease
Non-candidates for a complete CABG, or candidates for a complete CABG in whom, according to an expert panel, there is a high probability of failure of the grafts due to the extension and severity of the disease, with diffuse, small vessel involvement.
To provide a signed, written informed consent, according to the National Guidelines for Clinical Trials.

Exclusion criteria

Severe valve heart disease requiring surgical repair.
Serologic diagnostic of Chagas' disease.
Symptoms of heart failure, even from an ischemic etiology, in the absence of objectively documented myocardial ischemia.
Malignant ventricular arrhythmias (like VT), unless an ICD have been placed.
Any acute coronary syndrome in the past 3 months.
End-stage renal disease requiring maintenance dialysis.
History of neoplasia.
Drug or alcohol abuse.
Life expectancy below 2 years.
Enrollment in any cell therapy trial in the past 2 years.