Skip to content

Effects of Levosimendan on Diaphragm Function in Mechanically Ventilated Patients

Effects of Levosimendan on Diaphragm Function in Mechanically Ventilated Patients

Status
UNKNOWN
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01721434
Enrollment
42
Registered
2012-11-05
Start date
2012-09-30
Completion date
2016-05-31
Last updated
2015-06-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Muscle Weakness Conditions, Weaning Failure

Keywords

levosimendan, diaphragm function, mechanically ventilated patients, neuro-mechanical efficiency

Brief summary

Levosimendan is a relatively new drug that improves cardiac contractility in patients with heart failure. Its main mechanism of action is enhanced binding of calcium to the myocardial contractile proteins. Recent data from our lab showed that levosimendan improves contractility of human diaphragm in vitro (muscle fibers from COPD patient diaphragm) and in vivo (healthy subjects). Accordingly, levosimendan may appear of value in the treatment of disorders associated with impaired respiratory muscle function, such as mechanically ventilated patients.We hypothesize that levosimendan could improve respiratory muscle function in mechanically ventilated patients commencing a CPAP trial.

Interventions

DRUGLevosimendan
DRUGPlacebo

Similar coloured placebo

Sponsors

Orion Corporation, Orion Pharma
CollaboratorINDUSTRY
University Medical Center Nijmegen
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* mechanical ventilation \> 3 days * informed consent * able to sustain a CPAP trial for 30 minutes * PaO2/FiO2 ratio \> 200 mmHg * ventilatory settings: positive end expiratory pressure \<= 10 cmH2O, pressure support \<= 10 cmH2O

Exclusion criteria

* pre-existent muscle disease (congenital or acquired) or diseases/disorders known to be associated with myopathy including auto-immune diseases * pre-existent cardiac disease (based on history, electrocardiography and transthoracic echocardiography) * upper airway/esophageal pathology (i.e. recent surgery, esophageal varices, diaphragmatic hernia) * phrenic nerve lesions * pregnancy, breast feeding * severe renal failure (serum creatinine \> 150 umol/L) * severe hepatic failure * recent (within 5 days) nasal bleeding * systolic blood pressure \< 120 mmHg

Design outcomes

Primary

MeasureTime frameDescription
Neuro-mechanical efficiency of the diaphragmArtefact-free periode in the last 10 minutes of each CPAP trialThe primary outcome measure is the neuro-mechanical efficiency(i.e. the ratio of diaphragm electrical activity and transdiaphragmatic pressure) of the diaphragm during a continuous positive airway pressure (CPAP) trial.

Secondary

MeasureTime frameDescription
Oxygen consumption (VO2)Artefact-free periode in the last 10 minutes of each CPAP trialA secondary outcome measure is the oxygen consumption during a continuous positive airway pressure (CPAP) trial.
Partial pressure of oxygen in arterial blood (PaO2)Last minute of the 30 minute CPAP trialA secondary outcome measure is the PaO2 at the end of a continuous positive airway pressure (CPAP) trial.
Neuro-ventilatory efficiency of the diaphragmArtefact-free periode in the last 10 minutes of each CPAP trialA secondary outcome measure is the neuro-ventilatory efficiency (i.e. the ratio of diaphragm electrical activity and tidal volume) during a continuous positive airway pressure (CPAP) trial.
Carbon dioxide production (VCO2)Artefact-free periode in the last 10 minutes of each CPAP trialA secondary outcome measure is the carbon dioxide production during a continuous positive airway pressure (CPAP) trial.
Partial pressure of carbon dioxide in arterial blood (PaCO2)Last minute of the 30 minute CPAP trialA secondary outcome measure is the PaCO2 at the and of a continuous positive airway pressure (CPAP) trial.
Accessory respiratory muscle activityMeasured during a one hour protocol after the second CPAP trial.To determine the effects of levosimendan on accessory respiratory muscle function, ventilator settings are adapted after the last CPAP-trial.

Countries

Netherlands

Contacts

Primary ContactLeo MA Heunks, MD, PhD
l.heunks@ic.umcn.nl024-3617273
Backup ContactJonne Doorduin, MSc
j.doorduin@ic.umcn.nl024-3617273

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026