N/A
Completed N=37
Preoxygenation With Nasal Cannula and Noninvasive Positive Pressure Ventilation
Source: ClinicalTrials.gov NCT03093662 ↗Enrolled (actual)
37
Serious AEs
0.0%
Results posted
Dec 2020
Primary outcomePrimary: End-tidal Oxygen — 78.1; 78.6 End tidal oxygen saturation percentage
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.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY End-tidal Oxygen |
78.1; 78.6 | — |
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. Informational only — not medical advice.