drugset / Trial / NCT01536132
Intermittent Intravenous Levosimendan in Ambulatory Advanced Chronic Heart Failure Patients
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Levosimendan | Other / unclassified | 0.2 ug/kg | Intravenous |