Levosimendan in Acute Decompensated Heart Failure

Trial statusNot yet recruiting
Trial phasePhase 2, Phase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorChittagong Medical College

About this trial

Acute decompensated heart failure (ADHF) is one of the major causes of hospitalization and mortality worldwide. Despite advances in medical treatments, managing ADHF remains complex, especially in high-risk populations. Levosimendan, a calcium sensitizer that improves myocardial contractility and reduces complications associated with acute decompensated heart failure, has shown potential in improving outcomes in these patients. The present study aims to evaluate the efficacy and safety of levosimendan in patients with ADHF in a real-world clinical setting.

This pragmatic, multicenter, randomized, controlled trial will include adult patients diagnosed with ADHF in two groups: one receiving levosimendan infusion, and the other receiving standard care for heart failure management, according to the most up-to-date clinical protocols. The study is designed to assess both the efficacy and safety of levosimendan, comparing it with the current standard of care.

The primary endpoint of the study will be a clinical composite outcome measured from the NYHA functional classification of heart failure and patient global assessment. Secondary endpoints will include change in serum pro-BNP levels, clinical outcome of heart failure, changes in dyspnea status, all-cause and cardiac mortality. Safety endpoints, including adverse events, will also be systematically recorded and analyzed. Adverse events will be closely monitored, categorized as either mild, moderate, or severe, and their potential association with the treatment will be assessed.

Data collection will occur at baseline and during subsequent follow-up visits at 6 hours, 24 hours, 5 days (or day of discharge), and 90 days post-treatment. Key efficacy measures will be obtained through clinical evaluations and laboratory tests, including blood pressure, electrocardiogram (ECG) findings, and NT-proBNP serum levels. The statistical analysis will follow an intention-to-treat (ITT) and Per protocol (PP) approach to account for all enrolled patients, ensuring robust and generalizable findings. This study will be conducted in accordance with Good Clinical Practice (GCP) guidelines and ethical standards outlined in the Declaration of Helsinki, prioritizing participant safety and scientific rigor throughout the study.

12 The results of this trial will provide critical insights into the potential benefits of levosimendan for treating ADHF, and could potentially inform clinical decision-making, offering a more effective therapeutic option in managing this life-threatening condition.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adult patients (age >18 years)

Both male and female sex

Having left ventricular dysfunction, evidenced by a left ventricular ejection fraction <40% within the prior 12 months

Hospitalized for the treatment of ADHF

Disqualifiers

History of invasive cardiac procedure

Cardiac surgery during lifetime within 3 months prior to screening

Cardiac revascularization within 3 months prior to screening

Left ventricular assist device (LVAD) implantation within 3 months prior to screening

Trial design

Design model

Parallel

Treatments tested in this trial

  • Levosimendan

    Drug

    Levosimendan is a calcium-sensitizing inotrope with vasodilatory effects, enhancing heart contractility without raising oxygen demand and promoting vascular relaxation. In this trial, patients will be randomized to receive either standard care alone or standard care plus levosimendan (0.1 μg/kg/min IV infusion for 24 hours).

  • Standard care

    Other intervention

    Participants will receive standard care for acute decompensated heart failure according to the 2024 ACC Guideline for the Management of Heart Failure. This may include intravenous diuretics, vasodilators, inotropes, renin-angiotensin system inhibitors, beta-blockers, mineralocorticoid receptor antagonists, and SGLT2 inhibitors as clinically indicated.

Treatment groups

332 Participants
are divided into 2 treatment groups
Group A: Intervention ArmExperimental treatment 1 intervention
Group B: Standard CareActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Clinical Improvement in Heart Failure Symptoms

Improvement in heart failure symptoms during the first five days of treatment, categorized as improved (moderate or marked improvement at 6 hours, 24 hours, and 5 days without deterioration), unchanged (neither improved nor worsened), or worse (persistent unresponsive symptoms after 24 hours, need for rescue intervention, or moderate/marked worsening).

Time frame
From baseline to 5 days after treatment initiation

Secondary outcomes

1

Safety Outcomes - Adverse Events and Serious Adverse Events

Proportion of patients experiencing treatment-related adverse events and serious adverse events, classified by severity and relationship to study medication, monitored from infusion start until 24 hours post-infusion and at hospital discharge.

Time frame
From baseline to 90 days follow-up
2

Changes in Clinical and Functional Status

Changes in serum pro-BNP, patient global assessment scores, patient perception of dyspnea, Killip classification, and NYHA functional class measured at 24 hours, discharge, 30-day, and 90-day visits.

Time frame
From baseline to 90 days follow-up
3

Hospitalization and Mortality Outcomes

Length of hospital stay; in-hospital mortality; rehospitalizations within 90 days; cardiac mortality and all-cause mortality within 90 days.

Time frame
During index hospitalization and up to 90 days post-treatment initiation

Other outcomes

Sponsors and contacts

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Chittagong Medical College

Lead sponsor

Beacon Pharmaceuticals PLC

Collaborator

Pi Research and Development Center, Bangladesh

Collaborator

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