Effects of Levosimendan on Diaphragm Function in Mechanically Ventilated Patients
- Conditions
- Weaning FailureMuscle Weakness Conditions
- Interventions
- Drug: Placebo
- Registration Number
- NCT01721434
- Lead Sponsor
- University Medical Center Nijmegen
- 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 42
- 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
- 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
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Placebo Placebo Similar coloured placebo intravenous for a single 7 hours Levosimendan Levosimendan Levosimendan 0.2 ug/kg/min intravenous for a single 7 hours.
- Primary Outcome Measures
Name Time Method Neuro-mechanical efficiency of the diaphragm Artefact-free periode in the last 10 minutes of each CPAP trial The 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 Outcome Measures
Name Time Method Oxygen consumption (VO2) Artefact-free periode in the last 10 minutes of each CPAP trial A secondary outcome measure is the oxygen consumption during a continuous positive airway pressure (CPAP) trial.
Neuro-ventilatory efficiency of the diaphragm Artefact-free periode in the last 10 minutes of each CPAP trial A 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.
Partial pressure of carbon dioxide in arterial blood (PaCO2) Last minute of the 30 minute CPAP trial A secondary outcome measure is the PaCO2 at the and of a continuous positive airway pressure (CPAP) trial.
Partial pressure of oxygen in arterial blood (PaO2) Last minute of the 30 minute CPAP trial A secondary outcome measure is the PaO2 at the end of a continuous positive airway pressure (CPAP) trial.
Carbon dioxide production (VCO2) Artefact-free periode in the last 10 minutes of each CPAP trial A secondary outcome measure is the carbon dioxide production during a continuous positive airway pressure (CPAP) trial.
Accessory respiratory muscle activity Measured 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.
Trial Locations
- Locations (1)
Radboud University Nijmegen Medical Centre
🇳🇱Nijmegen, Gelderland, Netherlands