Treating COVID-19 With a Bidirectional Oxygenation Valve
NCT ID: NCT04326452
Last Updated: 2022-05-04
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
10 participants
INTERVENTIONAL
2020-03-27
2021-03-27
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Enrolled Subjects
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.
bidirectional oxygenation mouthpiece
Use of our bidirectional oxygenation mouthpiece with conventional oxygen support.
Interventions
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bidirectional oxygenation mouthpiece
Use of our bidirectional oxygenation mouthpiece with conventional oxygen support.
Eligibility Criteria
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Inclusion Criteria
* Able to provide informed consent
* Not currently requiring intubation
* Receiving oxygen by face mask
Exclusion Criteria
* Rapidly decompensating status requiring urgent or emergent higher level of care
18 Years
ALL
No
Sponsors
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PEEP Medical, LLC
INDUSTRY
TMC HealthCare
OTHER
Responsible Party
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Locations
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TMC HealthCare
Tucson, Arizona, United States
Stanford University
Stanford, California, United States
Emory Saint Joseph's Hospital
Atlanta, Georgia, United States
Countries
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Other Identifiers
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GO2 PEEP Study
Identifier Type: OTHER
Identifier Source: secondary_id
COVID19PEEP2020
Identifier Type: -
Identifier Source: org_study_id
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