Clinical Trials Directory

Trials / Completed

CompletedNCT00091507

IMMEDIATE Trial - Out of Hospital Administration of Glucose, Insulin and Potassium.

Immediate Myocardial Metabolic Enhancement During Initial Assessment and Treatment in Emergency Care Trial

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
911 (actual)
Sponsor
Tufts Medical Center · Academic / Other
Sex
All
Age
30 Years
Healthy volunteers
Not accepted

Summary

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).

Detailed description

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.

Conditions

Interventions

TypeNameDescription
DRUGGIKIntravenous solution, 1.5ml/kg/hour, continuous infusion for total of 12 hours.
DRUGPlaceboIntravenous solution of Dextrose 5 percent at 1.5 ml/kg/hour for a total of 12 hours.

Timeline

Start date
2006-11-01
Primary completion
2011-08-01
Completion
2012-08-01
First posted
2004-09-13
Last updated
2016-03-02
Results posted
2013-01-30

Locations

13 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00091507. Inclusion in this directory is not an endorsement.

IMMEDIATE Trial - Out of Hospital Administration of Glucose, Insulin and Potassium. (NCT00091507) · Clinical Trials Directory