drugset / Trial / NCT01188369

Effects of Levosimendan in Patients Eligible for Aortic Valve Replacement With Left Ventricular Hypertrophy

NCT01188369

Phase 4 Terminated 20 enrolled University of Aarhus
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a clinical, randomised, double-blinded study in which patients eligible for aortic valve replacement are enrolled. Patients receive infusion of either levosimendan or placebo 4 hours prior to surgery and until the end of surgery.

Timeline

Start
2010-09
Primary completion
2013-03
Completion
2013-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Levosimendan Other / unclassified 0.1 ug/kg Intravenous