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Clinical Trial Summary

The aim of the study is to compare the performance of the O3 cerebral oximeter and sensor to a 510(k) cleared NIRS (Near-Infrared Spectroscopy) device on neonatal subjects based on data collected from the cutaneously placed forehead sensors. Due to the design of the systems, the devices will be used serially instead of concurrently. Because of this timing, changes in patient state may not be reflected in measurements collected by both devices.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Regional Saturation of Oxygen (rSO2)

NCT number NCT03828487
Study type Interventional
Source Masimo Corporation
Contact
Status Terminated
Phase N/A
Start date December 19, 2018
Completion date June 14, 2019