CompletedPhase 3Phase 4ACTRN12610000280000

The NACIAM Study – Assessing the benefit of N-Acetylcysteine (NAC) in acute heart attacks.

The early use of N-Acetyl Cysteine In Acute Myocardial Infarction to assess the impact of early NAC therapy in reducing myocardial infarct size as determined by Cardiac Magnetic Resonance Imaging (CMRI).


Sponsor

The Queen Elizabeth Hospital Cardiology Unit

Enrollment

80 participants

Start Date

Mar 4, 2010

Study Type

Interventional

Conditions

Summary

N-Acetylcysteine (NAC) is an anti-oxidant which also potentiates the action of nitroglycerine. When used with nitrates in the context of acute myocardial infarction, it may reduce infarct size by minimising reperfusion injury as well as potentiating nitroglycerine's vasodilating and anti-platelet effects. The NACIAM trial is a randomised, double-blind, placebo-controlled study assessing the impact of early NAC therapy in reducing infarct size (as assessed by cardiac MRI) in patients with acute ST elevation myocardial infarction receiving intravenous nitrate therapy and undergoing primary percutaneous coronary intervention.


Eligibility

Sex: Both males and femalesMin Age: 18 Yearss

Inclusion Criteria1

  • Acute ST segment elevation myocardial infarction (STEMI) with primary percutaneous coronary intervention.

Exclusion Criteria3

  • Previous myocardial infarction.
  • Permanent pacemaker or implantable defibrillator (cardiac MRI contra-indicated).
  • Decision to administer open-label NAC for renoprotection

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Interventions

Intravenous (I.V.) N-Acetyl Cysteine (NAC) 15g or saline placebo in 500 mls 5% Dextrose delivered at 20 mg/min for 1st hour then 10 mg/min for next 47 hours. This is a one-off treatment.

Intravenous (I.V.) N-Acetyl Cysteine (NAC) 15g or saline placebo in 500 mls 5% Dextrose delivered at 20 mg/min for 1st hour then 10 mg/min for next 47 hours. This is a one-off treatment.


Locations(1)

Australia

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ACTRN12610000280000