Patient Self-Proning with High-Flow Nasal Cannula Improves Oxygenation in ARDS Patients: A Randomized Clinical Trial
Phase 1
Recruiting
- Conditions
- Respiratory
- Registration Number
- PACTR202204746577792
- Lead Sponsor
- Faculty of medicine Ain shams university
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 90
Inclusion Criteria
Mild ARDS
Age>18
BMI<30
Exclusion Criteria
Moderate to severe ARDS
Contraindications of proning e.g vitally instability
Immediate need of intubation
Refusal of prone position
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Our primary outcomes will be rate of intubation. End point of the study will be improvement of the patient or worsening of his condition and proceeding to intubation.<br><br>
- Secondary Outcome Measures
Name Time Method Our secondary outcomes will be measurement of complications of prone position and the period of ICU stay and mortality rate in the first 28 days of surgical ICU admission.