About this trial
The study aims to determine the effect of implementing cough augmentation techniques on weaning outcomes among critically ill patients
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
adult intubated patients
both sex
Disqualifiers
patient with facial trauma
patient with tracheostomy tube
Trial design
Parallel
Treatments tested in this trial
cough augmentation techniques
Other interventionthe lung volume recruitment maneuver via MV was applied with assistant of the attended physician as follows: Use pressure-controlled ventilation and increase end-inspiratory volume (30 or 40 cm H2O for 30 to 40 seconds unless contraindicated) or inspiratory hold for 30 to 40 seconds to promote cough effectiveness. The patient serially inhales a volume of gas without exhalation until maximum insufflation capacity via the ventilator to facilitate breath-holding (if not contraindicated).
Treatment groups
Trial outcomes
Primary outcomes
weaning success
measured through successful extubating
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
[email protected]
Lead sponsor
Damanhour University
Sponsor institution