MYSTAR-5-YEAR: Long-term Follow-up of Patients With Ischemic Heart Disease Treated With Cell Therapy (MYSTAR-5-YEAR)
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|ClinicalTrials.gov Identifier: NCT01395212|
Recruitment Status : Completed
First Posted : July 15, 2011
Last Update Posted : October 29, 2013
The MYSTAR-5-YEAR study controls the patients 5 years after treatment with combined (intramyocardial and intracoronary) delivery of autologous BM-MNCs.
The clinical endpoint of this prospective non-randomized observational study is the MACCE, defined as major adverse cardiac and cerebrovascular events. Patients will be investigated by echocardiography, SPECT and MRI. 2D (NOGA-guided SPECT) and 3D (NOGA-guided MRI) imaging will refine the evaluation with more exact analysis of the intramyocardial injected areas (ROI).
|Condition or disease|
|Acute Myocardial Infarction|
Background: Based on the available long-term results of cardiac stem cell therapies, it seems, that it offers short-term moderate benefits, but the long-term outcome is still matter of debate. In 2008, the Austrian arm of the MYSTAR study (a prospective multi-center single-blind trial) including patients with recent AMI and treated with combined (intramyocardial and intracoronary) delivery of autologous BM-MNCs has been completed with 1-year FUP. The MYSTAR results showed moderate but significant improvement in infarct size and LV function similar to other trials, and confirmed safety, feasibility and efficacy of BMC treatment in AMI patients. The patients enrolled in the study reach the 5 to 8 years FUP at 2011, raising the question whether the combined delivery of autologous BM-MNCs results in a long-term benefit for these patients.
Aim of the study: To investigate the long-term, 5 years clinical outcome of patients enrolled into the MYSTAR study.
Study design: Prospective non-randomized single-center Austrian long-term FUP registry.
Study patients: A total of 60 patients with previous cardiac stem cell therapy (participated in the MYSTAR study) will be included in the present study
Primary endpoint: occurrence of MACCE (major adverse cardiac and cerebrovascular events, including all-cause death, re-AMI, revascularization and stroke) during the mean 5 years follow-up.
Secondary endpoints: improvements of clinical symptoms, expressed as CCS and NYHA scores, change in global LV EF, measured by echocardiography, size of infarction determined by stress-rest SPECT, LV and RV volumes, function and cardiac output measured by cardiac MRI.
|Study Type :||Observational|
|Actual Enrollment :||60 participants|
|Official Title:||Long-term Follow-up of Patients With Ischemic Heart Disease Treated With Combined Delivery of Autologous Bone-marrow Mononuclear Cells: 5-year Clinical Outcome of the MYSTAR Study|
|Study Start Date :||July 2011|
|Actual Primary Completion Date :||May 2013|
|Actual Study Completion Date :||June 2013|
|Cardiac stem cell therapy 5 years ago|
- Occurrence of MACCE [ Time Frame: 5 years ]MACCE is defined as major adverse cardiac and cerebrovascular events including re-AMI, TVR, all-cause death and stroke at the 5-year FUP of the patients enrolled into the MYSTAR study and underwent cardiac stem cell therapy.
- Clinical symptoms (CCS, NYHA) [ Time Frame: 5 years ]
- Changes in global EF [ Time Frame: 5 years ]
- Size of infarction [ Time Frame: 5 years ]
- Left ventricular end-diastolic and end-systolic volumes [ Time Frame: 5 years ]
- Right ventricular end-diastolic and end-systolic volumes [ Time Frame: 5 years ]
- Right ventricular cardiac output [ Time Frame: 5 years ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01395212
|Medical University of Vienna|
|Vienna, Austria, A-1090|
|Principal Investigator:||Mariann Gyöngyösi, MD PhD||Medical University of Vienna|