Clinical Impact of Automated Oxygen Administration on Confirmed or Suspected COVID-19 in the Emergency Department.

Study Results

Results pending

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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Recruitment Status

UNKNOWN

Total Enrollment

60 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-02-28

Study Completion Date

2022-12-31

Brief Summary

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The aim of this study is to evaluate the impact of the FreeO2 system on the quality of the oxygen therapy in confirmed or suspected SARS-CoV-2 patients in the emergency department.

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Detailed Description

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The aim of this study is to evaluate the impact of the FreeO2 system on the quality of the oxygen therapy in confirmed or suspected SARS-CoV-2 patients in the emergency department. The quality of oxygen therapy is evaluated by the time spent in the SpO2 target (+/- 2% SpO2 target), time spent in hyperoxemia (\> 5% SpO2 target), time spent in hyperoxemia (\<5% SpO2 target).

Conditions

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COVID-19 Hypoxemia Hyperoxia Hypoxia

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Interventions

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Automated oxygen titration

Automated oxygen administration to maintain the SpO2 target at a predefined value during emergency length of stay

Intervention Type DEVICE

Other Intervention Names

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FreeO2 System TM, Oxy'nov.inc.

Eligibility Criteria

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Inclusion Criteria

* Hypoxemic patients on automated oxygen therapy during their emergency department stay
* Confirmed or suspected SARS-CoV-2 patients in the emergency department