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CompletedNCT04373161

Home Pulse Oximeter Use in Patients With COVID-19

Utilizing Home Pulse Oximetry for Patients With COVID-19 To Monitor Disease Progression

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
209 (actual)
Sponsor
Swedish Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to investigate the use of home pulse oximetry monitoring in patients with COVID-19 to trend disease progression and identify need for hospitalization.

Detailed description

This protocol studies patients with suspected non-severe Corona Virus Disease (COVID-19) being discharged to home from an emergency department (ED) or outpatient testing center. Patients will be provided a portable fingertip home pulse oximeter that measures peripheral oxygen saturation (SpO2). Patients will be instructed to check their resting home oxygen saturation three times per day and record these findings. They will be instructed to return to the emergency room for sustained oxygen saturation below 92% or if their symptoms are worsening and they feel they need medical attention. Patients will be called once daily by the research team to collect data in real time. Patients will be monitored for seven days, and at the end of the seven day period, they will return the pulse oximeter as well as a spreadsheet of their home oximetry readings. The purpose is to see if home pulse oximetry identifies disease progression and need for hospitalization in patients with COVID-19. Additionally, there will be analysis of trends in home oximetry readings wand predictors of morbidity and mortality.

Conditions

Interventions

TypeNameDescription
DEVICEHome Pulse Oximetry MonitoringPatients to check their home oxygen saturation three times daily and return to the ED for sustain oxygen \<92% or for worsening symptoms.

Timeline

Start date
2020-03-20
Primary completion
2020-04-22
Completion
2020-04-22
First posted
2020-05-04
Last updated
2020-05-06

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT04373161. Inclusion in this directory is not an endorsement.