Bidirectional Oxygenation Valve in the Management of Pulmonary Complications of COVID-19

Completed · Not applicable

Conditions studied: COVID-19

In brief

The objective of this study is to determine the safety, feasibility and efficacy of a bidirectional oxygenation Positive End Expiratory Pressure (PEEP) mouthpiece in coronavirus disease 2019 (COVID-19) patients requiring supplemental oxygen by non-rebreather mask.

Key facts

Study ID

NCT04331366

Run by

Emory University

People needed

2

Starts

2020-04-08

Expected to finish

2020-08-31

Last updated by the study team

2021-02-18

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• COVID-19 positive
• Oxygen saturation <92%
• Able to provide informed consent
• Receiving oxygen by non-rebreather mask
• Not currently requiring intubation

You may not qualify if…

• Unable or unwilling to provide informed consent
• Cognitive impairment
• Rapidly decompensating status requiring urgent or emergent higher level of care

Where it is running

• Emory University Hospital — Atlanta, Georgia, United States
• Emory St. Joseph's Hospital — Atlanta, Georgia, United States

Full record on ClinicalTrials.gov

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