Strengthening Transplantation Effects of Bone Marrow Mononuclear Cells With Atorvastatin in Myocardial Infarction

Myocardial Infarction Clinical Trial

— STEM-AMI  

Official title:

Strengthening Transplantation Effects of Bone Marrow Mononuclear Cells With Atorvastatin in Myocardial Infarction

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00979758
• Other study ID #: Fuwai Hospital 2009
• Status: Completed
• Phase: Phase 2
• First received: September 17, 2009
• Last updated: January 23, 2018
• Start date: January 2009
• Est. completion date: June 2016

Study information

• Verified date: January 2018
• Source: Chinese Academy of Medical Sciences, Fuwai Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The benefit of current stem cell transplantation therapy for myocardial infarction is limited by low survival rate for stem cell. The purpose of this study is to test whether intensive Atorvastatin therapy can improve the outcome of patients with impaired left ventricle function after myocardial infarction who underwent intracoronary transfer of autologous bone marrow cells.

Description:

The major challenge to a successful stem cell therapy for myocardial infarction is the low survival rate of implanted cells in the damaged tissue. Atorvastatin, an HMG-CoA reductase inhibitor, has multiple biological activities independent of cholesterol-lowering action.This study is performed to find out more information about the strategy with Atorvastatin therapy to improve the survival of implanted cells. autologous bone marrow stem cells transplantation. Patients between 30 and 80 years of age who receive autologous bone marrow stem cell transplant at the Fuwai cardiovascular hospital may be eligible for this study. These patients receive autologous bone marrow cells transplantation intracoronary undergoing Percutaneous Coronary Intervention with regular or high dose of Atorvastatin treatment. The objective evaluations will be performed at baseline and during 12 months follow-up.

Heart function tests may include the following:

1. Electrocardiogram (EKG) evaluates the electrical activity of the heart. Electrodes placed on the chest transmit information from the heart to a machine.

2. Echocardiogram (Echo) is an ultrasound test that uses sound waves to create an image of the heart and examine the function of the heart chambers and valves.

3. Gated acquisition scan is a nuclear medicine test that uses a small amount of radioactive chemical injected into a vein. A special scanner creates an image of the heart for examining the beating motion of the muscle.

4. MRI evaluates function of the heart chambers the beating motion of the muscle.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 100
• Est. completion date: June 2016
• Est. primary completion date: June 2015
• Accepts healthy volunteers: No
• Gender: All
• Age group: 30 Years to 80 Years

Eligibility

Inclusion Criteria:

1. Patients with coronary disease undergoing PCI.

2. At most 2 months since last episode of ST-elevation myocardial infarction.

3. Left ventricular ejection fraction >=20% <=45% based on coronary angiography or echocardiography.

Exclusion Criteria:

Any one of the following exclusion criteria is sufficient to disqualify a patient from the study.

1. Patients with non-ST-elevation myocardial infarction.

2. Patients with normal left ventricular function.

3. Patients with mechanical complications of myocardial infarction.

4. Patients with a malignant tumor.

5. Patients with infection disease.

6. Less than 6 months since last episode of stroke.

7. Patients with hematological disease (leukemia, myeloproliferative disease, or myelodysplastic syndromes).

8. AST (GOT) exceeding 100 IU/L or ALT (GPT) exceeding 100 IU/L.

9. Leukocytes less than 4,000/µL or exceeding 10,000/µL.

10. Platelets less than 100,000/µL.

11. Hemoglobin less than 10 g/dL.

12. Pregnant or nursing patients, those who may be pregnant, or those who plan on becoming pregnant before the end of the study period.

13. Any other reason that the Clinical Supervisors or Clinical Researchers may have for considering a case unsuitable for the study.

Related Conditions & MeSH terms

• Angioplasty, Transluminal, Percutaneous Coronary
• Infarction
• Myocardial Infarction
• Stem Cell Transplantation

Intervention

Drug:
• Atorvastatin and mononuclear cells transplantation
Routine or intensive dose of Atorvastatin therapy and mononuclear cells transplantation

Locations

Country	Name	City	State
China	Fuwai Hospital	Beijing

Sponsors (1)

Lead Sponsor	Collaborator
Chinese Academy of Medical Sciences, Fuwai Hospital

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Changes in left ventricular ejection fraction from baseline to 12 months' follow-up		12 months