NTX Wireless Patient Monitoring System

NCT00654693 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 26

Last updated 2012-09-07

No results posted yet for this study

Summary

* Determine the accuracy of the NTX wireless monitoring system alerts
* Evaluate patient compliance with wearing device
* Determine false alarm rates

Conditions

Interventions

OTHER

Rapid Response Team

If the subject is experiencing a life threatening change in their vital signs, the Rapid Response Team will be initiated per VUMC protocol.

Sponsors & Collaborators

  • Vanderbilt University

    lead OTHER

Principal Investigators

  • James M Berry, M.D. · Vanderbilt University Medical Center

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-03-31
Primary Completion
2009-01-31
Completion
2009-06-30

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00654693 on ClinicalTrials.gov