Effects of Levosimendan on Diaphragm Function in Mechanically Ventilated Patients

University Medical Center Nijmegen

Status and phase: Unknown; Phase 3; Phase 2

Conditions: Weaning Failure; Muscle Weakness Conditions

Treatments: Drug: Placebo; Drug: Levosimendan

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT01721434

Levo2

Details and patient eligibility

About

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.

Enrollment: 42 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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42 participants in 2 patient groups, including a placebo group

Levosimendan

Experimental group

Description:

Levosimendan 0.2 ug/kg/min intravenous for a single 7 hours.

Treatment:

Drug: Levosimendan

Placebo

Placebo Comparator group

Description:

Similar coloured placebo intravenous for a single 7 hours

Treatment:

Drug: Placebo