This study will utilize a single center internal control study design. The objective of this study is to determine the feasibility and safety of a bidirectional oxygenation PEEP generating mouthpiece when combined with oxygen by non-rebreather face mask, compared to support by oxygen non-rebreather face mask alone.
We have developed a simple and straightforward silicone rubber-made oral appliance that
promotes positive expiratory airway pressures with the potential to enhance respiratory
function while preventing and reversing atelectasis and hypoxia. The purpose of this study is
to compare the use of our bidirectional oxygenation mouthpiece with conventional oxygen
support versus conventional oxygen support of any Person Under Investigation for infection by
the COVID-19 virus.
Device: bidirectional oxygenation mouthpiece
Use of our bidirectional oxygenation mouthpiece with conventional oxygen support.
Inclusion Criteria:
- Oxygen saturation <93%
- Able to provide informed consent
- Not currently requiring intubation
- Receiving oxygen by face mask
Exclusion Criteria:
- Unable or unwilling to provide informed consent, cognitive impairment
- Rapidly decompensating status requiring urgent or emergent higher level of care
TMC HealthCare
Tucson, Arizona, United States
Stanford University
Stanford, California, United States
Emory Saint Joseph's Hospital
Atlanta, Georgia, United States