Levosimendan Compassionate Use in Pediatric Patients With Advanced Decompensated Heart Failure

NCT02973620 · Status: NO_LONGER_AVAILABLE · Type: EXPANDED_ACCESS

Last updated 2018-05-16

No results posted yet for this study

Summary

Open label study of levosimendan; planned comparison for effectiveness and safety to historic matched case controls from participating sites.

Conditions

  • Heart Decompensation

Interventions

DRUG

Levosimendan

levosimendan infusion started at 0.1 mcg/kg/min for 6-12 hours, increased to 0.2 mcg/kg/min for 24-36 hours

Sponsors & Collaborators

  • Tenax Therapeutics, Inc.

    lead INDUSTRY

Eligibility

Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02973620 on ClinicalTrials.gov