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Documentation of Hemoglobin Kinetics in Response to Mircera® in Patients With Acute Myocardial Infarction (BEAT-STEMI Pilot) (BEATSTEMIPi)

NCT01093820 Phase 2 COMPLETED

Hypothesis: Based on available pharmacokinetic data from healthy volunteers we hypothesize that the administration of a cumulative dose of 210μg of the continuous erythropoietin receptor activator, Mircera® (Roche), during 3 months post percutaneous coronary intervention (PCI) does not result in hemoglobin (Hb) levels \>15 g/dl in patients with ST-segment elevation myocardial infarction (STEMI) Design: Prospective, open label single center pilot study

Details

Lead sponsorUniversity Hospital, Basel, Switzerland
PhasePhase 2
StatusCOMPLETED
Enrolment8
Start date2010-04
Completion2010-10

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Interventions

Primary outcomes

Countries

Switzerland