The purpose of this study is to test the impact of pharmacological myocardial metabolic support, in the form of intravenous (IV) glucose, insulin and potassium (GIK), for the treatment of patients with threatened or established acute myocardial infarction (AMI).
BACKGROUND: Basic and clinical research suggests intravenous GIK metabolic myocardial support reduces ischemia-induced arrhythmias, progression from unstable angina pectoris (UAP) to acute myocardial infarction (AMI), myocardial infarction (MI) size, and mortality. Also, for ST elevation MI (STEMI), GIK may prolong time of benefit of coronary reperfusion. These effects should reduce short- and long-term mortality from ACS, including AMI and UAP, and the propensity for heart failure (HF). These benefits are related to the earliness of ACS, when both risk and opportunity to save lives are highest. DESIGN NARRATIVE: This is a randomized, placebo-controlled, double-blinded, multicenter clinical trial of IMMEDIATE GIK as early as possible in ACS in the prehospital emergency medical service (EMS) setting. Distinct from prior and ongoing GIK trials, this will test GIK for all ACS rather than only for AMI or STEMI in prehospital EMS. The primary hypothesis is that early GIK will prevent or reduce the size of acute myocardial infarction. Major secondary hypotheses posit GIK will reduce mortality (30 days and 1 year), reduce pre- or in-hospital cardiac arrest and the propensity for heart failure. Other hypotheses address mechanisms of these effects.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
911
Anchorage Site
Anchorage, Alaska, United States
New Haven Site
New Haven, Connecticut, United States
Macon Site
Macon, Georgia, United States
Progression of Acute Coronary Syndrome to Myocardial Infarction
Outcome for all participants during the first 24 hours of hospitalization; evidence of myocardial infarction is determined by ECG and biomarker results.
Time frame: 24 hours
Cardiac Arrest
Outcome for all participants who had a cardiac arrest from initial contact in the prehospital setting through their subsequent hospitalization.
Time frame: 1 to 18 hours (From prehospital setting through hospitalization.)
Heart Failure or Death
Outcome for all participants (composite of re-hospitalization for heart failure or death within 30 days)
Time frame: 30 days
Mortality
Outcome for all participants (mortality at 30 days).
Time frame: 30 days
Cardiac Arrest or Acute Mortality
Outcome for all participants (composite of cardiac arrest or acute mortality)
Time frame: Prehospital setting through hospitalization
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Brockton Site
Brockton, Massachusetts, United States
Concord Site
Concord, Massachusetts, United States
St. Paul Site
Saint Paul, Minnesota, United States
Albuquerque Site
Albuquerque, New Mexico, United States
Hershey Site
Hershey, Pennsylvania, United States
Sioux Falls Site
Sioux Falls, South Dakota, United States
Dallas Site
Dallas, Texas, United States
...and 3 more locations