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IMMEDIATE Trial: Immediate Myocardial Metabolic Enhancement During Initial Assessment and Treatment in Emergency care Trial - Article


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Diclofenac Potassium

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Clinical Trial: IMMEDIATE Trial: Immediate Myocardial Metabolic Enhancement During Initial Assessment and Treatment in Emergency care Trial

This study is not yet open for patient recruitment.

Sponsored by: National Heart, Lung, and Blood Institute (NHLBI)
Information provided by: National Heart, Lung, and Blood Institute (NHLBI)

Purpose

To study the effects of early administration of glucose, insulin, and potassium (GIK) in reducing mortality in acute coronary syndromes.

Condition Treatment or Intervention
Angina, Unstable
Cardiovascular Diseases
Heart Diseases
Coronary Disease
Myocardial Infarction
Heart Failure
 Drug: Glucose-Insulin-Potassium (GIK)

MedlinePlus related topics:  Angina;   Cardiomyopathy;   Coronary Disease;   Heart Attack;   Heart Diseases;   Heart Diseases--Prevention;   Vascular Diseases

Study Type: Interventional
Study Design: Prevention, Randomized, Placebo Control

Further Study Details: 

Study start: September 2004;  Expected completion: August 2009

BACKGROUND: Basic and clinical research suggest intravenous glucose, insulin, and potassium (GIK) metabolic myocardial support reduces ischemia-induced arrhythmias, progression from unstable angina pectoris I (UAP) to acute myocardial infarction (AMI), 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 acute coronary syndromes (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: IMMEDIATE is a randomized placebo-controlled clinical trial of immediate glucose, insulin, potassium (GIK) as early as possible in acute coronary syndrome (ACS): in the prehospital emergency medical service (EMS) setting, or, for those presenting to emergency departments (EDs), immediately upon ED arrival. Distinct from prior and ongoing GIK trials, this will test GIK for all ACS rather than only for AMI (or STEMI), and its use in prehospital EMS and ED settings. The primary hypothesis is that early GIK will reduce 30-day and 1-year mortality. Major secondary hypotheses posit GIK will reduce pre/in-hospital cardiac arrest, progression of unstable angina pectoris (UAP) to AMI, and by this and limiting MI size, will reduce the propensity for HF. Other hypotheses address mechanisms of these effects. The project will take 5 years: a year preparing and testing operations, 28 months enrolling patients, and then completion of data collection, analysis, and reporting. Clinical sites will be in Massachusetts, Texas, and Wisconsin.

Eligibility

Genders Eligible for Study:  Both

Criteria

No eligibility criteria

Location Information

Study chairs or principal investigators

Ralph D'Agostino,  New England Medical Center Hospitals   
Harry Selker,  New England Medical Center Hospitals   
James Udelson,  New England Medical Center Hospitals   

More Information

Study ID Numbers:  165
Record last reviewed:  March 2005
Last Updated:  March 24, 2005
Record first received:  September 9, 2004
ClinicalTrials.gov Identifier:  NCT00091507
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005

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December 2, 2009



Page Updated: June 1, 2005
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