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Clinical Trials/NCT04927078
NCT04927078
Completed
Not Applicable

Analysis of Vital Signs in Patients With COVID-19

Oxehealth Limited1 site in 1 country20 target enrollmentApril 1, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Respiratory Disease
Sponsor
Oxehealth Limited
Enrollment
20
Locations
1
Primary Endpoint
Breathing rates
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

This project will use data obtained from a proprietary vision-based patient monitoring and management system (OxeVision) for measuring heart rate and respiratory rate which is in clinical use at the Coventry and Warwickshire Partnership NHS Trust.

Detailed Description

The investigators will analyse data from patients with known COVID 19 infection both during, and where possible before clinical COVID 19 infection and controls to determine whether changes can be detected in these parameters that precede overt clinical deterioration. The role of remote vision-based patient monitoring and management in supporting the care of patients with COVID-19 will be assessed through staff interviews.

Registry
clinicaltrials.gov
Start Date
April 1, 2020
End Date
October 31, 2020
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Oxehealth Limited
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients age 18 and above. Patients on wards with a medical diagnosis of COVID 19 who are in rooms with the Vision based patient monitoring and management system.

Exclusion Criteria

  • Children will be excluded. No data will be excluded unless specifically requested by the treating clinician.

Outcomes

Primary Outcomes

Breathing rates

Time Frame: Data will be collected throughout study completion, an average of 7 months, to obtain breathing rate before and after the diagnosis of COVID 19.

Breathing rates collected via remote monitoring of participants using the Vision Based Patient Monitoring and Management System.

Secondary Outcomes

  • BR and PR(Data will be collected throughout study completion, an average of 7 months, to obtain breathing and pulse rate before and after the diagnosis of COVID 19.)
  • Pulse rates(Data will be collected throughout study completion, an average of 7 months, to obtain pulse rate before and after the diagnosis of COVID 19.)

Study Sites (1)

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