Effect of Implementing Cough Augmentation Techniques on Weaning Outcomes Among Critically Ill Patients

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
Sponsor[email protected]

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 volunteers

Qualifiers

adult intubated patients

both sex

Disqualifiers

patient with facial trauma

patient with tracheostomy tube

Trial design

Design model

Parallel

Treatments tested in this trial

  • cough augmentation techniques

    Other intervention

    the 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

88 Participants
are divided into 2 treatment groups
Group A: Interventional groupExperimental treatment 1 intervention
Group B: conventional groupNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

weaning success

measured through successful extubating

Time frame
within 7 days

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

[email protected]

Lead sponsor

Damanhour University

Sponsor institution