Stopped: Business decision with slower than expected enrollment..
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.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
NIBP measurements with no technical alarms/INOPs
Timeframe: 1 Visit
NIBP measurements with Diastolic, Systolic, and mean pressure within a physiologically plausible range for the patient population, treatment, and medication
Timeframe: 1 Visit
NIBP measurements with pulse pressure greater than 20% of the systolic blood pressure
Timeframe: 1 visit