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Levosimendan Administration in Pulmonary Hypertension (Levosim-PH)

Primary Purpose

Hypertension, Pulmonary, Cardiac Failure, Pulmonary Vascular Resistance Abnormality

Status
Completed
Phase
Not Applicable
Locations
Greece
Study Type
Interventional
Intervention
levosimendan at a dose of 3 mcg/kg
levosimendan at a dose of 6 mcg/kg
levosimendan at a dose of 12 mcg/kg
Sponsored by
Aretaieion University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Hypertension, Pulmonary focused on measuring pulmonary vascular resistance, pulmonary hypertension, vasodilators, cardiopulmonary bypass

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • patients with pulmonary hypertension due to left ventricular dysfunction based on echocardiographic diagnosis preoperatively
  • elective cardiac surgery

Exclusion Criteria:

  • primary pulmonary hypertension
  • thromboembolic disease
  • chronic obstructive pulmonary disease
  • emergency surgery
  • redo surgery
  • inability to consent to the study

Sites / Locations

  • Onassis Cardiac Surgery Center

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

levosimendan administration at a dose of 3 mcg/kg after anesthesia induction

levosimendan administration at a dose of 6 mcg/kg after anesthesia induction

levosimendan administration at a dose of 12 mcg/kg after anesthesia induction

Arm Description

levosimendan will be administered at a dose of 3 mcg/kg after anesthesia induction

levosimendan will be administered at a dose of 6 mcg/kg after anesthesia induction

levosimendan will be administered at a dose of 12 mcg/kg after anesthesia induction

Outcomes

Primary Outcome Measures

change from baseline in mean pulmonary arterial pressure (MPAP)
a Swan-Ganz catheter will be used for hemodynamic measurements

Secondary Outcome Measures

change from baseline in pulmonary vascular resistance (PVR)
a Swan-Ganz catheter will be used for hemodynamic measurements
change from baseline in mean arterial pressure (MAP)
a Swan-Ganz catheter will be used for hemodynamic measurements
change from baseline in systemic vascular resistance (SVR)
a Swan-Ganz catheter will be used for hemodynamic measurements
change from baseline in pulmonary capillary wedge pressure (PCWP)
a Swan-Ganz catheter will be used for hemodynamic measurements
change from baseline in cardiac output (CO)
a Swan-Ganz catheter will be used for hemodynamic measurements
change from baseline in tricuspid annular plane systolic excursion (TAPSE)
transthoracic and transesophageal echocardiography will be used for echocardiographic measurements
change from baseline in fractional area change
transthoracic and transesophageal echocardiography will be used for echocardiographic measurements

Full Information

First Posted
October 18, 2020
Last Updated
February 5, 2023
Sponsor
Aretaieion University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04599816
Brief Title
Levosimendan Administration in Pulmonary Hypertension
Acronym
Levosim-PH
Official Title
Levosimendan Administration in High Risk Cardiac Surgery Patients With Pulmonary Hypertension
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Completed
Study Start Date
October 17, 2020 (Actual)
Primary Completion Date
October 17, 2022 (Actual)
Study Completion Date
October 17, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Aretaieion University Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of the study is to examine the pharmacokinetics and pharmacodynamic properties of Levosimendan in cardiac surgery patients with pulmonary hypertension and impaired right ventricular function.
Detailed Description
Pulmonary hypertension (PH) is a pathophysiological disorder hemodynamically characterized by increased pulmonary vascular resistance and pressure. This can lead to right ventricle pressure overload and failure which is worsened by cardiopulmonary bypass (CPB) and extracorporeal circulation and is accompanied by high rates of morbidity and mortality in cardiac surgery patients. Pharmacological agents used to decrease pulmonary vascular resistance and right ventricle afterload are prostaglandins, iloprost, milrinone, nitric oxide (NO) and recently Levosimendan. These agents can be administered intravenously or via inhalation. In this study, Levosimendan will be administered in patients with pulmonary hypertension undergoing cardiac surgery. The aim of the study is to examine the pharmacokinetics and pharmacodynamic properties of Levosimendan in cardiac surgery patients with pulmonary hypertension and impaired right ventricular function. The drug will be administered in different doses to define the dose at which Levosimendan administration reduces pulmonary vascular resistance and pressure without causing significant reduction of systemic vascular resistance and pressure. The anti-inflammatory effect of the perioperative use of Levosimendan in cardiac surgery will also be studied. In this setting, 45 patients with PH caused by left sided heart disease, will be assigned into three groups: GROUP A: Administration of Levosimendan at a dosage of 3mcg/kg after anesthesia induction. GROUP B: Administration of Levosimendan at a dosage of 6mcg/kg after anesthesia induction. GROUP C: Administration of Levosimendan at a dosage of 12mcg/kg after anesthesia induction. Before and after the administration of the drug, heart function will be evaluated by hemodynamic measurements obtained by the Swan-Ganz catheter. These parameters will be heart rate (HR), blood pressure (BP), mean pulmonary arterial pressure (MPAP), central venous pressure (CVP), cardiac output (CO), pulmonary capillary wedge pressure (PCWP), cardiac index (CI), systemic vascular resistance (SVR), pulmonary vascular resistance (PVR). Transthoracic echocardiography (TTE) and transoesophageal echocardiography (TOE) will also be used. The anti-inflammatory action of Levosimendan will also be evaluated by interleukin-6 (IL-6) measurements. This study will lead to conclusions regarding the effectiveness of Levosimendan administration in the treatment of right heart failure and PH in cardiac surgery patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypertension, Pulmonary, Cardiac Failure, Pulmonary Vascular Resistance Abnormality
Keywords
pulmonary vascular resistance, pulmonary hypertension, vasodilators, cardiopulmonary bypass

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
45 (Actual)

8. Arms, Groups, and Interventions

Arm Title
levosimendan administration at a dose of 3 mcg/kg after anesthesia induction
Arm Type
Active Comparator
Arm Description
levosimendan will be administered at a dose of 3 mcg/kg after anesthesia induction
Arm Title
levosimendan administration at a dose of 6 mcg/kg after anesthesia induction
Arm Type
Active Comparator
Arm Description
levosimendan will be administered at a dose of 6 mcg/kg after anesthesia induction
Arm Title
levosimendan administration at a dose of 12 mcg/kg after anesthesia induction
Arm Type
Active Comparator
Arm Description
levosimendan will be administered at a dose of 12 mcg/kg after anesthesia induction
Intervention Type
Drug
Intervention Name(s)
levosimendan at a dose of 3 mcg/kg
Intervention Description
levosimendan will be administered intravenously at a dose of 3 mcg/kg after anesthesia induction
Intervention Type
Drug
Intervention Name(s)
levosimendan at a dose of 6 mcg/kg
Intervention Description
levosimendan will be administered intravenously at a dose of 6 mcg/kg after anesthesia induction
Intervention Type
Drug
Intervention Name(s)
levosimendan at a dose of 12 mcg/kg
Intervention Description
levosimendan will be administered intravenously at a dose of 12 mcg/kg after anesthesia induction
Primary Outcome Measure Information:
Title
change from baseline in mean pulmonary arterial pressure (MPAP)
Description
a Swan-Ganz catheter will be used for hemodynamic measurements
Time Frame
20 minutes after levosimendan administration, at the end of surgery and 2 hours after Intensive Care Unit (ICU) admission
Secondary Outcome Measure Information:
Title
change from baseline in pulmonary vascular resistance (PVR)
Description
a Swan-Ganz catheter will be used for hemodynamic measurements
Time Frame
20 minutes after levosimendan administration, at the end of surgery and 2 hours after Intensive Care Unit (ICU) admission
Title
change from baseline in mean arterial pressure (MAP)
Description
a Swan-Ganz catheter will be used for hemodynamic measurements
Time Frame
20 minutes after levosimendan administration, at the end of surgery and 2 hours after Intensive Care Unit (ICU) admission
Title
change from baseline in systemic vascular resistance (SVR)
Description
a Swan-Ganz catheter will be used for hemodynamic measurements
Time Frame
20 minutes after levosimendan administration, at the end of surgery and 2 hours after Intensive Care Unit (ICU) admission
Title
change from baseline in pulmonary capillary wedge pressure (PCWP)
Description
a Swan-Ganz catheter will be used for hemodynamic measurements
Time Frame
20 minutes after levosimendan administration, at the end of surgery and 2 hours after Intensive Care Unit (ICU) admission
Title
change from baseline in cardiac output (CO)
Description
a Swan-Ganz catheter will be used for hemodynamic measurements
Time Frame
20 minutes after levosimendan administration, at the end of surgery and 2 hours after Intensive Care Unit (ICU) admission
Title
change from baseline in tricuspid annular plane systolic excursion (TAPSE)
Description
transthoracic and transesophageal echocardiography will be used for echocardiographic measurements
Time Frame
20 minutes after levosimendan administration, at the end of surgery, 2 hours after Intensive Care Unit (ICU) admission and 80 hours after levosimendan administration
Title
change from baseline in fractional area change
Description
transthoracic and transesophageal echocardiography will be used for echocardiographic measurements
Time Frame
20 minutes after levosimendan administration, at the end of surgery, 2 hours after Intensive Care Unit (ICU) admission and 80 hours after levosimendan administration
Other Pre-specified Outcome Measures:
Title
change from baseline in blood levels of levosimendan
Description
blood levels will be measured with liquid chromatography
Time Frame
20 minutes, 6 hours, 12 hours, 24 hours and 80 hours after administration
Title
change from baseline in blood levels of interleukin-6 (IL-6)
Description
blood levels will be measured with the enzyme linked immunosorbent assay (ELISA)
Time Frame
end of surgery, 6 hours, 12 hours and 24 hours after Intensive Care Unit (ICU) admission

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients with pulmonary hypertension due to left ventricular dysfunction based on echocardiographic diagnosis preoperatively elective cardiac surgery Exclusion Criteria: primary pulmonary hypertension thromboembolic disease chronic obstructive pulmonary disease emergency surgery redo surgery inability to consent to the study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kassiani Theodoraki, PhD, DESA
Organizational Affiliation
Aretaieion University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Onassis Cardiac Surgery Center
City
Athens
ZIP/Postal Code
17674
Country
Greece

12. IPD Sharing Statement

Citations:
PubMed Identifier
12419726
Citation
Theodoraki K, Rellia P, Thanopoulos A, Tsourelis L, Zarkalis D, Sfyrakis P, Antoniou T. Inhaled iloprost controls pulmonary hypertension after cardiopulmonary bypass. Can J Anaesth. 2002 Nov;49(9):963-7. doi: 10.1007/BF03016884.
Results Reference
background
PubMed Identifier
28717881
Citation
Theodoraki K, Thanopoulos A, Rellia P, Leontiadis E, Zarkalis D, Perreas K, Antoniou T. A retrospective comparison of inhaled milrinone and iloprost in post-bypass pulmonary hypertension. Heart Vessels. 2017 Dec;32(12):1488-1497. doi: 10.1007/s00380-017-1023-2. Epub 2017 Jul 17.
Results Reference
background
PubMed Identifier
19151265
Citation
Haddad F, Couture P, Tousignant C, Denault AY. The right ventricle in cardiac surgery, a perioperative perspective: II. Pathophysiology, clinical importance, and management. Anesth Analg. 2009 Feb;108(2):422-33. doi: 10.1213/ane.0b013e31818d8b92.
Results Reference
background
PubMed Identifier
29979110
Citation
Hansen MS, Andersen A, Nielsen-Kudsk JE. Levosimendan in pulmonary hypertension and right heart failure. Pulm Circ. 2018 Jul-Sep;8(3):2045894018790905. doi: 10.1177/2045894018790905. Epub 2018 Jul 6.
Results Reference
background
PubMed Identifier
18496375
Citation
Boost KA, Hoegl S, Dolfen A, Czerwonka H, Scheiermann P, Zwissler B, Hofstetter C. Inhaled levosimendan reduces mortality and release of proinflammatory mediators in a rat model of experimental ventilator-induced lung injury. Crit Care Med. 2008 Jun;36(6):1873-9. doi: 10.1097/CCM.0b013e3181743e63.
Results Reference
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PubMed Identifier
30052230
Citation
Kundra TS, Nagaraja PS, Bharathi KS, Kaur P, Manjunatha N. Inhaled levosimendan versus intravenous levosimendan in patients with pulmonary hypertension undergoing mitral valve replacement. Ann Card Anaesth. 2018 Jul-Sep;21(3):328-332. doi: 10.4103/aca.ACA_19_18.
Results Reference
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PubMed Identifier
30612930
Citation
Elhassan A, Essandoh M. Inhaled Levosimendan for Pulmonary Hypertension Treatment During Cardiac Surgery: A Novel Application to Avoid Systemic Hypotension. J Cardiothorac Vasc Anesth. 2019 Apr;33(4):1169-1170. doi: 10.1053/j.jvca.2018.11.039. Epub 2018 Nov 28. No abstract available.
Results Reference
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PubMed Identifier
17631672
Citation
Zhang J, Gage EM, Ji QC, El-Shourbagy TA. A strategy for high-throughput analysis of levosimendan and its metabolites in human plasma samples using sequential negative and positive ionization liquid chromatography/tandem mass spectrometric detection. Rapid Commun Mass Spectrom. 2007;21(14):2169-76. doi: 10.1002/rcm.3046.
Results Reference
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Levosimendan Administration in Pulmonary Hypertension

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