A single bolus EPO administered just before a primary PCI for a first acute myocardial infarction will increase left ventricular function after 4 months.
ID
Bron
Verkorte titel
Aandoening
One group will receive the study medication and the other group will receive placebo medication.
Ondersteuning
Van Buchem Stichting (UMCG)
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
The main study endpoint will be left ventricular ejection faction, measured with Cardiac Magnetic Resonance Imaging at 4 months after onset of the acute myocardial infarction.
Achtergrond van het onderzoek
Erythropoetin (EPO) is commonly known as an effective treatment for anemia, (partly) caused by an inadequate production of endogenous EPO (e.g., renal failure). However, we and others suggested several important extra-hematopoeitic effects of EPO, which might be beneficial in the setting of an acute myocardial infarction. Recent animal studies provided very consistent evidence for a reduced infarct size and improved left ventricular function caused by EPO administration. In addition, we and others have mainly explained the beneficial effects of EPO by non-hematopoietic effects, such as reduction of apoptosis and stimulation of neovascularisation.
Clinical studies with EPO in non-anemic patients are scarce. However, in our safety study, EPO administration in patients with an acute myocardial infarction was safe and well tolerated. Therefore the primary objective of this study is to establish the effects of a single bolus EPO administered just before a primary PCI for a first acute myocardial infarction, on left ventricular function after 4 months.
Doel van het onderzoek
A single bolus EPO administered just before a primary PCI for a first acute myocardial infarction will increase left ventricular function after 4 months.
Onderzoeksproduct en/of interventie
1. One bolus of EPO (Eprex, about 60.000 IU) will be administered intravenously in 30 minutes, within 3 hours after the primary PCI procedure. OR
2. Placebo
Publiek
P.O. Box 30001
J. Hogenhuis
Groningen 9700 RB
The Netherlands
+31 (0)50 3618061
j.hogenhuis@thorax.umcg.nl
Wetenschappelijk
P.O. Box 30001
J. Hogenhuis
Groningen 9700 RB
The Netherlands
+31 (0)50 3618061
j.hogenhuis@thorax.umcg.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
Successful primary PCI (TIMI 2/3) for a first acute myocardial infarction, diagnosed by:
1. Chest pain suggestive for acute myocardial infarction;
2. Symptom onset < 12 hour after hospital admission, or < 24 hour in case ongoing ischemia;
3. ECG with ST-T segment elevation > 1 mV in 2 or more leads;
4. TIMI flow 0/1 before primary PCI on diagnostic coronary angiography.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
1. Hemoglobin levels > 10.6 mmol/L;
2. Anticipated additional revascularisation within 4 months;
3. Cardiogenic shock;
4. Presence of other serious medical conditions;
5. Pregnancy/breast feeding;
6. Malignant hypertension;
7. End stage renal failure (kreatinin > 220 micromol/l);
8. Previous treatment with rh-EPO;
9. Blood transfusion <12 weeks prior to randomisation;
10. Allergy against rh-EPO;
11. Polycytemia verae;
12. Previous acute myocardial infarction;
13. Concomitant inflammatory or malignant disease;
14. Recent trauma or major surgery;
15. Unwilling to sign informed consent;
16. Contra-indications for MRI (pacemaker and other metal subjects).
Opzet
Deelname
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Geen registraties gevonden.
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
| Register | ID |
|---|---|
| NTR-new | NL619 |
| NTR-old | NTR678 |
| Ander register | : N/A |
| ISRCTN | ISRCTN46528154 |