Hypertension Clinical Trial
Official title:
A Pilot Study to Evaluate the Performance of Nihon Kohden's NTX Wireless Patient Monitoring System
- Determine the accuracy of the NTX wireless monitoring system alerts
- Evaluate patient compliance with wearing device
- Determine false alarm rates
Approximately 150 patients will have wireless monitors attached to their arm. They will have
their vital signs filtered through software that generates alerts and records data. The
alert engine will produce pager and application based pop-up alerts which will be sent to
the research nurse. Low and high limit alarms will be set according to the published
guidelines (Hillman, K. et. Al., Resuscitation 48(2): 105-10, 2001) and adjusted at will by
the response team.
During this portion of the study, the following research related procedures will be
performed:
- begin continuous vital signs monitoring (BP - 1x per hour, 3 lead ECG -continuous, HR -
continuous, SpO2 - continuous)
- PI or Co-PI will review each alert that's generated. The clinical significance will be
determined and recorded in the study database
- Record patient's signs and symptoms daily
- Assess concomitant
- Assess AE's, SAEs
;
Observational Model: Cohort, Time Perspective: Prospective
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