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Completed
NCT03129217
The Validity of Maximal Diaphragm Thickening Fraction to Measure Diaphragm Function in Mechanically Ventilated Patients
Conditions: Diaphragm Injury, Weaning Failure, Mechanical Ventilation Complication
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Enrollment: 29
Sponsor: University Health Network, Toronto
Location: University Health Network Toronto Ontario
Summary
This study is designed to determine whether maximal diaphragm thickening fraction measured by ultrasound during volitional maximal inspiratory efforts is a valid measure of diaphragm function in mechanically ventilated patients.
Eligibility Criteria
Inclusion Criteria:
* Adult patients (≥ 18 years old) with acute respiratory failure receiving invasive mechanical ventilation via endotracheal tube or tracheostomy
* Patients who meet readiness-to-wean criteria (triggering the ventilator; FiO2 ≤ 50%; PEEP ≤ 8 cm H20; hemodynamic stability)
Exclusion Criteria:
* Contraindication to phrenic nerve stimulation (chest tube; cardiac pacemaker or implanted defibrillator; cervical implants; use of neuromuscular blocking agents within the 24 hours preceding the first diaphragm assessment (with the exception of succinylcholine used during rapid-sequence induction of anaesthesia for intubation); cervical spine injury; known pregnancy)
* Patients experiencing an acute exacerbation of an obstructive lung disease (chronic obstructive pulmonary disease (COPD), asthma, bronchiectasis)
Source: ClinicalTrials.gov (NCT03129217). StuddyBuddy aggregates publicly available trial information.