Cardiovascular Magnetic Resonance for the Occluded Infarct-Related Artery Treatment (COAT)

This study has been terminated.
(The study was prematurely terminated due to low enrollment.)
Sponsor:
Information provided by (Responsible Party):
Institute of Cardiology, Warsaw, Poland
ClinicalTrials.gov Identifier:
NCT00968383
First received: June 30, 2009
Last updated: November 5, 2012
Last verified: November 2012

June 30, 2009
November 5, 2012
September 2009
December 2012   (final data collection date for primary outcome measure)
change in systolic wall thickening (SWT) [ Time Frame: 6 months ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00968383 on ClinicalTrials.gov Archive Site
  • change in left ventricular ejection fraction (LVEF) [ Time Frame: 6 months ] [ Designated as safety issue: No ]
  • change in wall motion score index (WMSI) [ Time Frame: 6 months ] [ Designated as safety issue: No ]
  • change in left ventricular end-diastolic volume (LVEDV) [ Time Frame: 6 months ] [ Designated as safety issue: No ]
  • change in left ventricular end-systolic volume (LVESV) [ Time Frame: 6 months ] [ Designated as safety issue: No ]
  • myocardial tissue characteristics [ Time Frame: 3-5 days ] [ Designated as safety issue: Yes ]
Same as current
Not Provided
Not Provided
 
Cardiovascular Magnetic Resonance for the Occluded Infarct-Related Artery Treatment
Late Percutaneous Coronary Intervention of the Occluded Infarct-Related Artery in Patients With Preserved Infarct Zone Viability Determined With Magnetic Resonance Imaging

The purpose of this study is to determine whether opening an occluded infarcted artery 3-28 days after an acute myocardial infarction in high-risk asymptomatic patients with preserved infarct zone viability improves left ventricular systolic function and volumes at 6 months follow-up. The secondary purpose is to assess the changes in myocardial tissue characteristics after late percutaneous coronary intervention (PCI).

Rapid restoration of blood flow in the infarct-related artery (IRA), one of the cornerstones of contemporary treatment of acute myocardial infarction (MI) prevents myocardial necrosis and its consequences. However, due to late presentation or failed fibrinolytic therapy up to one third of patients have persistently occluded IRA after MI.

Recently, the Occluded Artery Trial (OAT) has demonstrated that percutaneous coronary intervention (PCI) with optimal medical therapy does not reduce the frequency of major adverse events compared to optimal medical therapy alone when performed on days 3-28 post MI in stable patients. Assessment of infarct zone viability was not used as an inclusion/exclusion criterion in the main OAT trial.

Several studies confirm that patients with left ventricular systolic dysfunction and preserved myocardial viability (necrosis transmurality<50% in most segments of the infarct zone) assessed with magnetic resonance imaging benefit from revascularization.

Late opening of the occluded infarct-related artery only in patients with preserved myocardial tissue viability may lead to improvement of left ventricular volumes and function.

Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
  • Cardiovascular Diseases
  • Heart Diseases
  • Myocardial Infarction
  • Heart Failure
  • Drug: Beta adrenergic blockers
    Participants will receive beta adrenergic blockers.
  • Drug: Platelet inhibitors
    Participants will receive platelet inhibitors.
  • Drug: Statins
    Participants will receive statins.
  • Drug: ACE inhibitors and/or ARB and/or AA
    Participants will receive ACE inhibitors and/or ARB and/or AA
  • Procedure: PCI with stenting
    Participants will undergo percutaneous coronary intervention (PCI) and coronary stenting.
  • Active Comparator: Optimal medical therapy
    Conventional medical management, including aspirin, clopidogrel, statins, beta blockers, angiotensin converting enzyme (ACE) inhibitors and/or angiotensin receptor blocker (ARB) and/or aldosterone antagonist and risk factor modification
    Interventions:
    • Drug: Beta adrenergic blockers
    • Drug: Platelet inhibitors
    • Drug: Statins
    • Drug: ACE inhibitors and/or ARB and/or AA
  • Experimental: PCI with optimal medical therapy
    Conventional medical management, including aspirin, clopidogrel, statins, beta blockers, angiotensin converting enzyme (ACE) inhibitors and/or angiotensin receptor blocker (ARB) and/or aldosterone antagonist and risk factor modification plus percutaneous coronary intervention and coronary stenting
    Interventions:
    • Drug: Beta adrenergic blockers
    • Drug: Platelet inhibitors
    • Drug: Statins
    • Drug: ACE inhibitors and/or ARB and/or AA
    • Procedure: PCI with stenting

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Terminated
11
December 2012
December 2012   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Enrollment 3-28 days after an acute myocardial infarction.
  • Infarct related artery occlusion (TIMI 0 or 1).
  • High risk: left ventricular ejection fraction (LVEF)<50% or LVEF>50% and proximal coronary occlusion.
  • Preserved infarct zone viability (necrosis transmurality <50% in at least 4 segments out of 17 according to AHA classification).

Exclusion Criteria:

  • Unstable clinical condition
Both
18 Years to 85 Years
No
Contact information is only displayed when the study is recruiting subjects
Poland
 
NCT00968383
2.50/V/09
No
Institute of Cardiology, Warsaw, Poland
Institute of Cardiology, Warsaw, Poland
Not Provided
Principal Investigator: Lukasz A Malek, M.D. PhD Institute of Cardiology, Warsaw, Poland
Study Chair: Mariusz Kruk, M.D. PhD Institute of Cardiology, Warsaw, Poland
Study Chair: Mariusz Klopotowski, M.D. Institute of Cardiology, Warsaw, Poland
Institute of Cardiology, Warsaw, Poland
November 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP