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Completed

NCT Number: NCT01538771

Intracoronary Darbepoetin-alpha to Reduce The Infarct Size and Post-Infarct Remodeling

Prospective, randomized and open label trial

Hypothesis

* Infusion of intracoronary darbepoetin-alpha at the time of reperfusion may reduce infarct size and post-infarct pathologic left ventricular remodeling in patients with ST-segment elevation myocardial infarction.

Methods

* Randomization into control group or treatment group * Treatment group : Darbepoetin-alpha 300ug intracoronary bolus infusion via over-the-wire balloon system simultaneously with first balloon inflation and conventional treatment * Control group : conventional treatment

Endpoints

* peak CK-MB & troponin levels : baseline,6h,12hr,18hr, 24hr, 36hr and 48hr * MRI at baseline : infarct size, area at risk and salvaged myocardium * MRI at 4 months : prevalence of pathologic left ventricle remodeling (definition: increase of end-diastolic volume index > 20% compared to baseline) * safety endpoint : cardiac death, nonfatal myocardial infarction, stent thrombosis, ischemic stroke, hospital readmission with heart failure or ischemic symptom, bleeding and urgent target lesion revascularization

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Seoul National University Bundang Hospital

Seongnam, 463707, South Korea

About this study

[Eligibility Criteria]

  • Patients, regardless of gender, at the age from 18 to 80 years were eligible if they had within 12 hours of onset of ST-segment myocardial infarction that was decided to treat with primary percutaneous coronary intervention.

[Exclusion criteria]

  • Uncontrolled congestive heart failure (Killip classes II and III, or cardiogenic shock)
  • History of malignancy
  • Serious hematological disease
  • Current infectious disease requiring antibiotic therapy
  • Baseline creatinine level > 2.0 mg/dL or dependence on dialysis
  • Known hypersensitivity to or contraindication for heparin, aspirin, clopidogrel, sirolimus, everolimus, contrast medium and darbepoetin-α

[Primary endpoint] Myocardial infarct size, estimated by measurement of peak levels of cardiac biomarker (CK-MB and troponin-I of the patients was followed for 48 hours at every 6 hours)

[Secondary end points]

  • The infarct size, measured as the area of delayed enhancement seen with cardiac magnetic resonance (CMR) imaging on average four days after ST-segment elevation myocardial infarction (baseline)
  • The proportion of area at risk (AAR) and salvaged myocardium, calculated by formula; [AAR - Infarct size] / AAR X 100 (%)
  • The change of left ventricular ejection fraction (LVEF), LV end-diastolic volume (LVEDV), and LV end-systolic volume (LVESV) assessed by CMR between four days and four months
  • LV remodeling index [(LVEDV at four months - baseline LVEDV) / baseline LVEDV X 100%] and the incidence of pathologic LV remodeling (LV remodeling index > 20%);

[Safety endpoints] The incidence of composites of the cardiovascular endpoints (cardiac death, nonfatal myocardial infarction, stent thrombosis, ischemic stroke, hospital readmission with heart failure or ischemic symptoms, bleeding and urgent target lesion revascularization) assessed at four months.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients with ST-elevation myocardial infarction (MI) within 12 hours of onset
  • Suitable coronary anatomy for PCI
  • Age < 80 yrs

Exclusion criteria

  • Uncontrolled congestive heart failure (Killip classes II and III, or cardiogenic shock)
  • History of malignancy
  • Serious hematological disease
  • Current infectious disease requiring antibiotic therapy
  • Baseline creatinine level > 2.0 mg/dL or dependence on dialysis
  • Known hypersensitivity to or contraindication for heparin, aspirin, clopidogrel, sirolimus, everolimus, contrast medium and darbepoetin-α

Treatment and study plan

darbepoetin alfa

Drug

Darbepoetin alfa 300ug intracoronary bolus infusion via over-the-wire balloon before the 1st ballooning and conventional treatment

Other names: Nesp PFS Prefilled Syringe (Jeilkirin Pharm. Korea)

Control saline

Drug

Same volume of saline intracoronary bolus infusion via over-the-wire balloon before the 1st ballooning and conventional treatment

Other names: 0.9% normal saline

Primary outcomes

  1. Peak CK-MB/ Troponin-I levels

    Time frame: baseline, 6, 12,18,24,36,48hrs

Secondary outcomes

  1. Infarct size, area at risk and proportion of salvaged myocardium

    Time frame: Participants will be followed for the duration of hospital stay, an expected average of 4 days

    Assessed by cardiac MRI

  2. Pathologic left ventricle remodeling assessed by cardiac MRI

    Time frame: 4 months

    Definition : Increase of end-diastolic volume of left ventricle >20%

  3. Change of left ventricular ejection fraction, LV end-diastolic volume , and LV end-systolic volume assessed by cardiac MRI

    Time frame: Between four days and 4 months

  4. Composites of cardiovascular endpoints

    Time frame: 4 Months

    ccardiac death, nonfatal myocardial infarction, stent thrombosis, ischemic stroke, hospital readmission with heart failure or ischemic symptoms, bleeding and target lesion revascularization

Sponsors and collaborators

Lead sponsor

Seoul National University Bundang Hospital

Other

Registry information

Official study title

The Efficacy of IntraCoronary Erythropoietin Delivery BEfore Reperfusion: Gauging Infarct Size in Patients With Acute ST-segment Elevation Myocardial Infarction (ICEBERG).

Important dates

Study start
2009
Primary completion
2012
Study completion
2013
First posted
Feb 24, 2012
Registry last updated
Jun 19, 2015

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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