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.
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.
| Condition | Movement, Involuntary |
|---|---|
| Treatment | Philips IntelliVue X3 patient monitor with investigational NIBP measurement algorithm (measured once per 3 minutes) |
| Clinical Study Identifier | NCT05185037 |
| Sponsor | Philips Clinical & Medical Affairs Global |
| Last Modified on | 30 March 2023 |
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