N/A
N=37
Preoxygenation With Nasal Cannula and Noninvasive Positive Pressure Ventilation
Hypoxia
Bottom Line
View on ClinicalTrials.gov: NCT03093662 ↗Enrolled (actual)
37
Serious AEs
0.0%
Results posted
Dec 2020
Primary outcome: Primary: End-tidal Oxygen — 78.1; 78.6 End tidal oxygen saturation percentage
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Ventilation with nasal cannula (Device); Ventilation without nasal cannula (Device)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Brooke Army Medical Center
- Primary completion
- Mar 2017
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY End-tidal Oxygen |
78.1; 78.6 | — |
Summary
This is a prospective randomized cross over study of healthy volunteers comparing end-tidal oxygen concentration among subjects undergoing continuous positive airway pressure ventilation via a noninvasive ventilation (NIV) mask with and without the addition of nasal cannulas.
Eligibility Criteria
Inclusion Criteria
- Any healthy volunteer aged 18-65 years.
Exclusion Criteria
- Previous inability to tolerate noninvasive positive pressure ventilation with addition of a nasal cannula.
- Known underlying cardiac or pulmonary disease.
- Active respiratory infections.
Data sourced from ClinicalTrials.gov (NCT03093662). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.