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Completed

NCT Number: NCT01388504

Nitrites in Acute Myocardial Infarction

The research question to be addressed is "Does a 2.5 - 5 minute systemic intravenous injection of sodium nitrite administered immediately before opening of the infarct related artery result in significant reduction of ischaemia reperfusion injury in patients with first acute ST elevation myocardial infarction (MI)?"

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

Aberdeen Royal Infirmary, Aberdeen, United Kingdom

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About this study

There are estimated to be 125,000 acute myocardial infarctions (heart attacks) in the UK every year. Although substantial progress has been made in reducing the infarct size by prompt opening of the infarct related artery (with thrombolytic therapy or percutaneous coronary intervention (PCI)), effective therapy to further reduce the infarct size would substantially reduce the risk of the patient subsequently developing heart failure.

There is a growing body of evidence from studies in animals that the use of nitrites may help in reducing the infarct size, although this has not been tested in man.

In this phase 2/3 study, the investigators propose to investigate the effect of sodium nitrite injection on infarct size. Eligible patients will be males aged 18 and over and females aged 55 and over, presenting within 12 hours of the onset of chest pain, who are suitable for treatment with percutaneous coronary intervention. Those who give verbal agreement to take part will receive a 2.5-5 minute injection of sodium nitrite (or placebo) immediately prior to the blocked artery being opened with percutaneous coronary intervention.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Men aged ≥18 years, women aged ≥55 years, and women <55years who are sterilised, or have had a hysterectomy or have effective contraception and thus where there is no possibility of them being pregnant; presenting within 12 hours of the onset of chest pain who have ST segment elevation of more than 1mm elevation in limb leads or 2mm elevation in two contiguous chest leads or new left bundle branch block (LBBB) and for whom the clinical decision has been made to treat with primary PCI will be eligible for enrolment. Occlusion of the culprit related artery (TIMI grade 0 or TIMI grade 1) will also be required for inclusion. Eligible patients will be of North European descent.

Exclusion criteria

  • Historical or ECG evidence of previous myocardial infarction
  • Patients with prior coronary artery bypass grafting (CABG)
  • Prior revascularization procedure where this procedure (PCI) was performed in the same territory as the current infarct
  • Known or suspected pregnancy
  • Contra-indications to MRI
  • Patients with cardiac arrest or cardiogenic shock
  • Patients with left main coronary occlusion
  • Patients with known moderate to severe renal failure (estimated GFR < 30mls/min), or liver failure
  • Patients with prior thrombolysis for this event
  • Patients with such Left Main disease which after PCI of their culprit lesion (culprit lesions may be located in the LAD or LCx or RCA) are likely to require CABG within the time course of the study period (6 months).

Treatment and study plan

Sodium Nitrite

Drug

sterile solution containing low dose sodium nitrite dissolved in 5ml water injected intravenously over a period of 2½ - 5 minutes immediately prior to opening of the infarct related artery using Percutaneous Coronary Intervention

Placebo

Other

sterile solution containing 0.9%w/v sodium chloride in 5ml water injected intravenously over a period of 2½ - 5 minutes immediately prior to Percutaneous Coronary Intervention

Primary outcomes

  1. Infarct size corrected for area at risk (using ESA)

    Time frame: 6-8 days post injection

Secondary outcomes

  1. Left ventricular ejection fraction and end systolic volume index

    Time frame: 6-8 days and 6 months post injection

  2. Plasma creatine kinase

    Time frame: 72 hours post injection

  3. Troponin I

    Time frame: 72 hours post injection

  4. Infarct size corrected for area at risk

    Time frame: 6 months

  5. Infarct size corrected for area at risk (using T2)

    Time frame: 6-8 days

Sponsors and collaborators

Lead sponsor

University of Aberdeen

Other

Collaborators

  • Brighton and Sussex University Hospitals NHS Trust
  • Imperial College London
  • Medical Research Council
  • NHS Grampian
  • St George's Healthcare NHS Trust
  • University of Birmingham

Registry information

Official study title

Does Sodium Nitrite Administration Reduce Ischaemia-reperfusion Injury in Patients Presenting With Acute ST Segment Elevation Myocardial Infarction?

Acronym: NIAMI

Important dates

Study start
2011
Primary completion
2014
Study completion
2014
First posted
Jul 6, 2011
Registry last updated
Jan 21, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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