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Clinical Trial Summary

This prospective cohort study will determine the diagnostic accuracy of the Owlet OSS 3.0 monitor for the detection of episodes of bradycardia and/or hypoxemia among infants.


Clinical Trial Description

We will attach an Owlet monitor to infants for a 48-hour period. We will prospectively collect data from this device to determine the accuracy of bradycardia and hypoxemia detection compared with hospital monitors. In addition, we will collect simultaneous high-resolution real time cardiorespiratory data from Philips MP70 patient monitors at the University of Alabama at Birmingham. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05774470
Study type Observational
Source University of Alabama at Birmingham
Contact
Status Completed
Phase
Start date April 22, 2023
Completion date July 29, 2023

See also
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Completed NCT02347241 - Infant Special Program for In Hospital Resuscitation Education in the Delivery Room N/A