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Completed Phase 3 Interventional Results available

Levosimendan in Patients With Left Ventricular Systolic Dysfunction Undergoing Cardiac Surgery On Cardiopulmonary Bypass

ClinicalTrials.gov ID: NCT02025621

Public ClinicalTrials.gov record NCT02025621. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 4:41 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Double-Blind, Randomized, Placebo-Controlled Study of Levosimendan in Patients With Left Ventricular Systolic Dysfunction Undergoing Cardiac Surgery Requiring Cardiopulmonary Bypass

Study identification

NCT ID
NCT02025621
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Tenax Therapeutics, Inc.
Industry
Enrollment
882 participants

Conditions and interventions

Interventions

  • Levosimendan Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 30, 2014
Primary completion
Oct 31, 2016
Completion
Oct 31, 2016
Last update posted
Jun 20, 2018

2014 – 2016

United States locations

U.S. sites
49
U.S. states
25
U.S. cities
44
Facility City State ZIP Site status
University of Alabama at Burlington Hospital Burlington Alabama
Huntsville Hospital Huntsville Alabama
Mercy General Hospital Sacramento California
University of California San Diego Medical Center San Diego California
Stanford University School of Medicine Stanford California
Hartford Hospital Hartford Connecticut
Yale-New Haven Hospital New Haven Connecticut
Boca Raton Community Hospital Boca Raton Florida
Shands Hospital at the University of Florida Gainesville Florida
Tampa General Hospital Tampa Florida
Redmond Regional Medical Center Rome Georgia
Northwestern University Hospital Evanston Illinois
Lutheran Hospital of Indiana Fort Wayne Indiana
Franciscan St. Francis Health Indianapolis Indiana
Iowa Heart Center/ Mercy Medical Center West Des Moines Iowa
University of Louisville Hospital Louisville Kentucky
Maine Medical Center Portland Maine
Brigham and Women's Hospital Boston Massachusetts
Tufts Medical Center Boston Massachusetts
St. Joseph's Mercy Hospital Ann Arbor Michigan
Oakwood Hospital and Medical Center Dearborn Michigan
Spectrum Health Grand Rapids Michigan
St. Luke's Hospital Kansas City Missouri
Barnes Jewish Hospital St Louis Missouri
Nebraska Heart Institute Lincoln Nebraska
Nebraska Medical Center Omaha Nebraska
Morristown Medical Center Morristown New Jersey
St. Peter's Hospital Albany New York
Columbia University Medical Center New York New York
Lenox Hill Hospital New York New York
Mount Sinai Medical Center New York New York
Saint Francis Hospital/The Heart Center Roslyn New York
Mission Hospital Asheville North Carolina
Moses H. Cone Memorial Hospital Greensboro North Carolina
Duke University Hospital Raleigh North Carolina
The Christ's Hospital; Lindner Clinical Trial Center Cincinnati Ohio
Case Medical Center Cleveland Ohio
Cleveland Clinic Cleveland Ohio
Ohio State University Hospital Columbus Ohio
ProMedica Toledo Hospital Toledo Ohio
Oklahoma Heart Hospital Oklahoma City Oklahoma
Lehigh Valley Hospital Allentown Pennsylvania
St. Thomas Heart Nashville Tennessee
Vanderbilt University Medical Center Nashville Tennessee
Baylor Hospital Dallas Texas
The Heart Hospital Baylor Plano Plano Texas
University of Virginia Health System Charlottesville Virginia
Franciscan Health System Res. Center Tacoma Washington
Aurora Saint Luke's Medical Center Milwaukee Wisconsin

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 11 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02025621, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 20, 2018 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02025621 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →