Acute Myocardial Infarction Clinical Trial
Official title:
Study of Stem Cell Therapy in Patients With Myocardial Infarction and Persistent Total Occlusion of Infarct Related Artery
Background: When an acute myocardial infarction occurs, the artery supplying the infarct
zone should be opened within twenty four hours of onset of infarction. This has clearly been
shown to be beneficial.
If the patient presents later than 24 hours of onset, at that stage a large part of the
damage to the heart is irreversible. Intervening at this stage (beyond 24 hours is
controversial). Some trials suggest that opening the artery even at this stage positively
modifies the remodeling process while other trials suggest that such a benefit is not seen.
Hypothesis: Opening an infarct related artery after 24 hours (until 6 months) and combining
it with intracoronary stem cell therapy may provide incremental benefit.It is possible that
the lack of benefit seen with late revascularization (>24 hrs) after MI may be offset by
giving intracoronary stem cells after opening the artery.
Objectives
The benefit of opening an infarct related artery after the period of myocardial salvage (In
patients who do not come to medical attention within 24 hrs of an infarctions) has been
questioned in recent trials. On the other hand, Stem cell therapy after myocardial
infarction has been shown to improve myocardial function both in the acute and chronic
phases. It is possible that the lack of benefit seen with late revascularization (>24 hrs)
after MI may be offset by giving intracoronary stem cells after opening the artery. Patients
with recent myocardial infarction (MI) and occluded infarct related arteries supplying a
large myocardial territory and with reduced ejection fraction will be randomized to a
percutaneous coronary intervention (PCI) arm and a PCI plus stem cell arm .
The objective of the trial is to demonstrate that opening an infarct related artery after 24
hours and before six months and following it with intracoronary stem cell therapy may
provide incremental benefit.
The primary objective
To demonstrate benefits in left ventricular recovery (improvement in function by
echocardiogram and Nuclear imaging: Multigated acquisition [MUGA], reduction in scar size by
tetrofosmin scan/Positron Emission Tomography[PET]. )
The secondary objectives
To demonstrate improvement in functional capacity as assessed by 6 minute walk test and
quality of life assessment, along with reduction of first occurrence of recurrent MI,
hospitalization/treatment of New York Heart Association class IV congestive heart failure,
or death
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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