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Clinical Trial Summary

The study intervention consists of a non-invasive blood pressure (NIBP) measurement device and cuff (FDA-cleared Philips IntelliVue X3 Rev. N.04 patient monitor) running a non-approved modified software containing an enhanced measurement algorithm for NIBP.


Clinical Trial Description

The purpose of this study is to compare measurements of NIBP taken by the study device and measurements taken by the current FDA-approved algorithm included in Rev. N.0 software for the IntelliVue patient monitors during motion artifact in patients undergoing caesarian section deliveries under epidural anesthesia. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05185037
Study type Observational
Source Philips Clinical & Medical Affairs Global
Contact Robert Jardin, BS, BSIT
Phone 612-500-1839
Email [email protected]
Status Not yet recruiting
Phase
Start date January 13, 2022
Completion date May 30, 2022

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