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The use of Helium in acute myocardial infarction trial (HAMI-trial).

Conditions
Acute myocardial infarctionacute coronary syndromeischemia reperfusion injuryacuut hartinfarctacuut coronair syndroomischemie reperfusie schade
Registration Number
NL-OMON23814
Lead Sponsor
Academical Medical Center, University of Amsterdam
Brief Summary

/A

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Not specified
Target Recruitment
70
Inclusion Criteria

1. Age 18-75 years;

2. ST-elevation myocardial infarction;

Exclusion Criteria

1. Left bundle branch block;

2. Previous myocardial infarction;

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
On day 4 after the PCI a CMR will be obtained. T-2 weighed imaging shows edema in the tissue which has been ischemic before and is therefore at risk for developing infarction. T-1 weighed imaging after the injection of gadolinium contrast marks the infarcted tissue. Primary endpoint is the total volume of infarction as proportion of the total volume of myocardium at risk.
Secondary Outcome Measures
NameTimeMethod
CMR measurements:<br /><br>1. On day 2-4: Left ventricular function, left ventricular dimensions, infarct size, edema;<br /><br>2. After 4 months: Left ventricular function, left ventricular dimensions, infarct size;<br /><br>3. Biomarker release following the PCI: Troponin T, NT-proBNP;<br /><br>4. Time of ST-segment resolution after opening of the target vessel;<br /><br>5. Thrombolysis in myocardial infarction (TIMI);<br /><br>6. Grade Flow following opening of the target vessel;<br /><br>7. Occurrence of death, re-infarction and admission for heart failure at 30 days and 4 months following PCI;<br /><br>8. New York heart Association functional class at 30 days and 4 months following PCI.
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