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Stem Cell Therapy in Patients With Myocardial Infarction and Persistent Total Occlusion of Infarct Related Artery (COAT)

A

All India Institute Of Medical Science (AIIMS)

Status

Unknown

Conditions

Acute Myocardial Infarction

Treatments

Procedure: coronary dilatation and stenting
Procedure: Intracoronary stem cells injection

Study type

Interventional

Funder types

Other

Identifiers

NCT01625949
ICMR project 80/3/2010-BMS
I-676 (Other Grant/Funding Number)

Details and patient eligibility

About

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.

Full description

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

Enrollment

40 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Age:18 to 80 years
  2. Sex:Both
  3. Recent MI (3-28 d)
  4. Obstructed artery needing intervention
  5. consent for stem cell therapy

Exclusion criteria

  1. Left main disease or Triple vessel disease[TVD] needing surgery
  2. Hypotension
  3. Consent not given

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

40 participants in 2 patient groups

Control Arm (Standard Therapy)
Active Comparator group
Description:
Control Arm Receiving The Standard Therapy including successful coronary intervention and stenting
Treatment:
Procedure: coronary dilatation and stenting
Intracoronary stem cells
Experimental group
Description:
Intracoronary stem cells will be injected in the infarct related artery after a successful coronary dilatation and stenting
Treatment:
Procedure: Intracoronary stem cells injection

Trial contacts and locations

1

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Central trial contact

Sandeep Seth, DM; S Seth

Data sourced from clinicaltrials.gov

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