Effect of Implementing Cough Augmentation Techniques on Weaning Outcomes Among Critically Ill Patients
Recruiting
N/A
Interventional Study
Physiological Parameters
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Supportive Care
- Participants needed
- 88 (estimated)
- Sponsor
- Heba.Attia@nur.dmu.edu.eg · Other
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About This Trial
The study aims to determine the effect of implementing cough augmentation techniques on weaning outcomes among critically ill patients
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* adult intubated patients
* both sex
Exclusion Criteria:
* patient with facial trauma
* patient with tracheostomy tube
Contacts