Seoul National University Bundang Hospital
Seongnam, 463707, South Korea
NCT Number: NCT01538771
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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Notify Me18 year–80 year
All sexes
Interventional
Phase 2
Seongnam, 463707, South Korea
[Eligibility Criteria]
[Exclusion criteria]
[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]
[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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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)
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
Time frame: baseline, 6, 12,18,24,36,48hrs
Time frame: Participants will be followed for the duration of hospital stay, an expected average of 4 days
Assessed by cardiac MRI
Time frame: 4 months
Definition : Increase of end-diastolic volume of left ventricle >20%
Time frame: Between four days and 4 months
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
Seoul National University Bundang Hospital
Other
The Efficacy of IntraCoronary Erythropoietin Delivery BEfore Reperfusion: Gauging Infarct Size in Patients With Acute ST-segment Elevation Myocardial Infarction (ICEBERG).
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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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