Preoxygenation With Nasal Cannula and Noninvasive Positive Pressure Ventilation

Completed · Not applicable

Conditions studied: Hypoxia

In brief

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.

Key facts

Study ID

NCT03093662

Run by

Brooke Army Medical Center

People needed

37

Starts

2017-03-02

Expected to finish

2017-03-09

Last updated by the study team

2021-02-12

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Any healthy volunteer aged 18-65 years.

You may not qualify if…

• Previous inability to tolerate noninvasive positive pressure ventilation with addition of a nasal cannula.
• Known underlying cardiac or pulmonary disease.
• Active respiratory infections.

Where it is running

• Brooke Army Medical Center — Fort Sam Houston, Texas, United States

Full record on ClinicalTrials.gov

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