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Validation of the NTX Wireless Patient Monitoring System

NCT00644644 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1303

Last updated 2017-04-11

No results posted yet for this study

Summary

* Reduction in time to detection of Clinically Significant events
* Reduction of time to Intervention during Clinically Significant events
* Reduction in the number of admissions to Intensive Care

Conditions

Interventions

OTHER

Rapid Response Team (NTX wireless monitoring system)

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 Medical Center

    lead OTHER

Principal Investigators

  • Daniel J France, PhD, MPH · Vanderbilt University Medical Center

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-03-31
Primary Completion
2010-01-31
Completion
2010-01-31

Countries

  • United States

Study Locations

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Entities

Diseases

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 NCT00644644 on ClinicalTrials.gov