The LeoDOR trial is a randomized, double-blind, placebo-controlled protocol designed to evaluate the efficacy and safety of intermittent levosimendan therapy in patients with advanced heart failure.
RCT
double-blind
randomized
Yes
Does intermittent levosimendan therapy improve a hierarchical composite of clinical outcomes and NT-proBNP in patients following hospitalization for acute heart failure?
The LeoDOR trial protocol outlines a randomized study to evaluate the efficacy and safety of intermittent levosimendan infusions in patients recently hospitalized for acute heart failure.
Hospitalization for acute heart failure (HF) is associated with a substantial morbidity burden and with associated healthcare costs and an increased mortality risk. However, few if any major medical innovations have been witnessed in this area in recent times. Levosimendan is a first-in-class calcium sensitizer and potassium channel opener indicated for the management of acute HF. Experience in several clinical studies has indicated that administration of intravenous levosimendan in intermittent cycles may reduce hospitalization and mortality rates in patients with advanced HF; however, none of those trials were designed or powered to give conclusive insights into that possibility. This paper describes the rationale and protocol of LeoDOR (levosimendan infusions for patients with advanced chronic heart failure), a randomized, double-blind, placebo-controlled, international, multicentre trial that will explore the efficacy and safety of intermittent levosimendan therapy, in addition to optimized standard therapy, in patients following hospitalization for acute HF. Salient features of LeoDOR include the use of two treatment regimens, in order to evaluate the effects of different schedules and doses of levosimendan during a 12 week treatment phase, and the use of a global rank primary endpoint, in which all patients are ranked across three hierarchical groups ranging from time to death or urgent heart transplantation or implantation of a ventricular assist device to time to rehospitalization and, lastly, time-averaged proportional change in N-terminal pro-brain natriuretic peptide. Secondary endpoints include changes in HF symptoms and functional status at 14 weeks.
Pölzl et al. (Tue,) conducted a rct in advanced chronic heart failure. Levosimendan vs. placebo was evaluated on global rank primary endpoint across three hierarchical groups: time to death/urgent heart transplantation/VAD implantation, time to rehospitalization, and time-averaged proportional change in NT-proBNP. The LeoDOR trial is a randomized, double-blind, placebo-controlled protocol designed to evaluate the efficacy and safety of intermittent levosimendan therapy in patients with advanced heart failure.
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