Transepicardial With Transseptal Autologous CD 133+ Bone Marrow Cell Implantation in Patient Following CABG Surgery
Coronary Artery Disease

About this trial
This is an interventional treatment trial for Coronary Artery Disease focused on measuring CD 133+, Transepicardial with Transseptal Implantation, CABG
Eligibility Criteria
Inclusion Criteria:
- patients with coronary artery disease 3 vessels disease indicated for CABG
- LVEF < 35% which has been confirmed by MRI
- Patients with akinetic or hypokineic segment, and left ventricle myocardial hypoperfusion confirmed in MRI
- has signed informed consent
Exclusion Criteria:
Emergency CABG Ungraftable coronary artery Acute myocardial Infarct (<14 days) Valve disease which need surgery repair Contraindicated for MRI High degree ventricular arrhytmia Coagulation disorder HIV positive patient, Hepatitis B + patients, HCV + patients AST/ALT > 1,5 upper normal value Creatinine > 2 g/dl. Malignancy
Drop out criteria :
Aortic cross clamp >120 minutes and CABG total time >180
Sites / Locations
- National Cardiovascular Center Harapan Kita
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
subject
control
this arm will receive Transepicardial with Transseptal CD 133+ Implantation
this arm will not receive Transepicardial with Transseptal CD 133+ Implantation