drugset / Trial / NCT01536132

Intermittent Intravenous Levosimendan in Ambulatory Advanced Chronic Heart Failure Patients

NCT01536132

Phase 4 Completed 70 enrolled Parc de Salut Mar
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to determine the safety and efficacy of intravenous administration of intermittent doses of levosimendan (infusions of 0,2 μg/kg/min, of levosimendan or placebo, without bolus, for 6 hours every 2 weeks) compared to placebo in ambulatory patients with advanced chronic heart failure.

Timeline

Start
2010-04
Primary completion
2013-10
Completion
2015-11

Drugs

EvaluationDrugModalityDoseRoute
Comparator Levosimendan Other / unclassified 0.2 ug/kg Intravenous

Indications