Overview

This trial is active, not recruiting.

Conditions chronic myocardial ischemia, left ventricular dysfunction
Treatment mesenchymal stem cells
Phase phase 1/phase 2
Sponsor University Hospital, Toulouse
Collaborator French Blood Establishment (Midi-Pyrénées)
Start date October 2009
End date February 2014
Trial size 10 participants
Trial identifier NCT01076920, 0505008

Summary

Ischemic cardiomyopathies are a leading cause of death in both men and women. When a person has a heart attack, blood is unable to reach a certain area of the heart, and if the blood supply is not re-established quickly, that area of the heart can suffer permanent damage. While recovery from a heart attack can be managed through medications and lifestyle changes, these treatments can not reverse the all damage to the heart. Current research is focusing on the development of cell-based therapies using stem cells to repair organs that have been irreversibly damaged by disease. A specific form of stem cells, called adult mesenchymal stem cells (MSCs), has shown promise for heart repair. This study will evaluate the safety of injecting MSCs directly into the heart to repair and restore heart function in people who have had a heart attack and who have chronic myocardial ischemia with heart failure.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Endpoint classification safety study
Intervention model single group assignment
Masking open label
Primary purpose treatment
Arm
(Experimental)
mesenchymal stem cells
60x106 MSCs Trans-endocardial intramyocardial injections (n=14-16)

Primary Outcomes

Measure
Evaluate safety and feasibility of transendocardial injection using the NogaStar XP Mapping Catheter with the MyostarTM Left Ventricular Injection Catheter of autologous MSC in subjects with chronic myocardial ischemia and left ventricular dysfunction
time frame: 30 days

Secondary Outcomes

Measure
Change from baseline in SF-36, VO2max, 6 min walk test, and the NYHA, CCS Classifications Effect related to cardiac function
time frame: 30 days to 2 years

Eligibility Criteria

Male or female participants at least 18 years old.

Inclusion Criteria: 1. Age 18 to 75 2. Male or female 3. NYHA (Heart failure) Class II-IV or Angina pectoris CCS Class III or IV or symptoms consistent with) 4. Chronic coronary artery disease with left ventricular function below 35% 5. Stable medical therapy for at least one month 6. Reversible perfusion defects by SPECT 7. Not a candidate for coronary artery by-pass surgery due to poor targets or small vessels and not a candidate for percutaneous intervention due to small vessels or unreachable coronary lesions due to complicated anatomy 8. Implantable Cardiovertor Defibrillator Exclusion Criteria: 1. Acute coronary syndrome, revascularization (PCI or CABG), or cardiac resynchronization during the last 3 months 2. Sustained ventricular 3. Further revascularization planned for the next 30 days. 4. Chronic atrial fibrillation. 5. A wall thickness in the target region <8 mm as determined by 2D echocardiography (the target region is defined at the time of NOGA® mapping). 6. An LV thrombus. 7. Severe peripheral vascular disease precluding femoral artery access as determined at time of original catheterization. 8. Aortic stenosis as determined as valve area less than 1 cm2 that prohibits catheter access to the LV. 9. Human immunodeficiency virus (HIV1-2), HTLV-1 and 2. 10. An active uncontrolled infection. 11. A prosthetic aortic valve. 12. A current or prior history within the last 3 years of neoplasm (excluding basal cell) and/or any active neoplasm within the last 24 months. 13. Pregnancy or breastfeeding. 14. Active participation in other research therapy for cardiovascular repair/regeneration. 15. Any medical condition that would affect the investigator's ability to evaluate the subject's condition or could compromise the subject's safety. 16. Any condition that, in the judgment of the investigator, would prohibit the subject from participating in the study.

Additional Information

Official title Administration of Mesenchymal Stem Cells in Patients With Chronic Ischemic Cardiomyopathy
Principal investigator jerome RONCALLI, MD, PhD
Description Mesenchymal stem cells from the bone marrow can differentiate into endothelial cells and participate in the development of new blood vessels in ischemic tissue. The aim of the study is in a phase I safety study to evaluate the clinical effect of autologous mesenchymal stem cell therapy in patients with severe chronic myocardial ischemia.10 patients with reversible ischemia on a SPECT will be treated with direct intramyocardial injections of autologous isolated and expanded mesenchymal stem cells.Clinical and objective evaluations will be performed at baseline and during 24 months follow-up.
Trial information was received from ClinicalTrials.gov and was last updated in December 2013.
Information provided to ClinicalTrials.gov by University Hospital, Toulouse.