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Clinical Trial 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


Clinical Trial Description

1200 patients will have wireless monitors attached to their arm. They will be randomized to have their vital signs filtered through software that generates alerts, or software that does not generate alerts. Low and high limit alarms will be set according to published guidelines and adjusted at will by the response team. If appropriate the Vanderbilt University Medical Center Rapid Response team will be initiated per Institutional Policy ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00644644
Study type Observational
Source Vanderbilt University Medical Center
Contact
Status Completed
Phase N/A
Start date March 2008
Completion date January 2010

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