Combined CABG and Stem-Cell Transplantation for Heart Failure

University of Helsinki

Status and phase: Unknown; Phase 2

Conditions: Coronary Artery Disease; Myocardial Infarction; Heart Failure

Treatments: Procedure: Bone marrow aspiration (crista iliaca); Biological: Intramyocardial injection of autologous serum; Biological: Intramyocardial mesenchymal stem cell transplantation; Procedure: Coronary bypass operation

Study type: Interventional

Funder types: Other

Identifiers

NCT00418418

TYH 6220

Details and patient eligibility

About

This is a prospective double blind trial of intraoperative transmyocardial bone marrow-derived mesenchymal cell transplantation vs placebo in patients with low left ventricular ejection fraction scheduled to coronary bypass operation.

Full description

The prevalence of symptomatic heart failure in general population is up to 2% and the prevalence increases rapidly with age. Half of the patients with symptomatic heart failure will die within 4 years of diagnosis.The purpose of this study is to examine the effect of bone marrow-derived stem cell transplantation in left ventricular ejection fraction.

Consecutive patients with systolic heart failure (n=60), with ischemic coronary heart disease, scheduled to by-pass-operation (CABG) will be collected from cardiovascular laboratory and outpatient clinic of Helsinki University Central Hospital. Patients should have heart failure with ejection fraction between 15 to 45%. Randomly patients are selected to receive a stem cell transplantation with best possible heart failure medication, or without cell transplantation. In this study, 30 patients are receiving bone marrow transplantation, and 30 patients are serving as a control population. All patients will receive CABG.The study will be carried out with randomized, double blind techniques for one year. Randomization (in blocks) will be based on a table of random numbers.Bone marrow and patients own serum will be blinded by using colored syringe, so that the doctor transfusing the sample, will not be able to know the nature of the sample. From all patients, a right atrial biopsy will be collected for assessment of autologous cardiac stem cells. Also sample of pericardial fluid will be collected for measures of growth factors.

Comparisons: Preoperatively, patients will be imagined by cardiac ultrasound, cardiac MRI, cardiac PET and SPECT. Serum pro-BNB samples will be collected. Postoperatively at 3 months and 6 months pro-BNB and cardiac ultrasound will be evaluated. At one year cardiac ultrasound, cardiac MRI, cardiac PET and SPECT will be reassessed.

Heart failure and coronary artery disease treatments beside the transplantation will be optimized according to the judgment of the doctors of the outpatients clinic. Primary endpoint of the study is the change of ejection fraction in MRI images.

Enrollment: 60 estimated patients

Sex: All

Ages: 18 to 75 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• General (patients must have all)

  • Symptomatic heart failure.
  • Scheduled to CABG
  • Be 18 to 75 years of age
  • Informed Consent obtained

• Heart Failure Presentation

  • Patients of either gender, who has evaluated in cardiovascular laboratory and scheduled to CABG with moderate heart failure, will be eligible
  • NYHA II-IV symptoms
  • Left ventricular ejection fraction in screening echocardiography 15 to 45%.
  • Optimal heart failure medication and coronary medication before operation, containing at least two heart failure drugs: must have ACE-inhibitor, or AT II blocker, and/or b-blocker together with diuretics, digitalis or aldosterone antagonist, and coronary medication: a statin and anticoagulation, either aspirin or clopidogrel.

Exclusion criteria

• Heart failure due to left ventricular outflow track obstruction (valve problem or HOCM)
• History of life-threatening ventricular arrhythmias or resuscitation, condition which may be repeatable or implanted ICD.
• Stroke or other disabling condition with in 3 months before screening
• Contraindications to coronary angiogram or MRI
• Other serious disease limiting life expectancy
• Participation in an other clinical trial
• Severe valve disease: mitral, aortic, tricuspid or pulmonic stenosis / insufficiency
• Scheduled valve operation

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Factorial Assignment

Masking: Quadruple Blind

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60 participants in 2 patient groups, including a placebo group

A

Active Comparator group

Description:

Patient group receiving the stem cell injections during the CABG

Treatment:

Procedure: Coronary bypass operation

Biological: Intramyocardial mesenchymal stem cell transplantation

Procedure: Bone marrow aspiration (crista iliaca)

B

Placebo Comparator group

Description:

The patient group receiving autologous serum injections during the CAGB operation

Treatment:

Procedure: Coronary bypass operation

Biological: Intramyocardial injection of autologous serum

Procedure: Bone marrow aspiration (crista iliaca)