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Clinical Trials/NCT01692847
NCT01692847
Completed
Not Applicable

Examination of the Impact of Better Surveillance and Communication of Patient Deterioration on Patient Related Outcomes (VitalCare - Guardian Version 2)

Philips Healthcare1 site in 1 country678 target enrollmentOctober 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Severe Sepsis
Sponsor
Philips Healthcare
Enrollment
678
Locations
1
Primary Endpoint
Improvement of outcome for patients after implementing the IGS
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

A hospitals manual method of patient monitoring will be implemented in an automated system and supported by an early patient deterioration detection for timely escalation. The purpose of this study is to assess if clinical outcomes of patients in Acute Care are significantly improved by such a system.

Detailed Description

The purpose of this study is to assess if the Philips IntelliVue Guardian Solution (IGS) with all its components can significantly improve clinical outcomes for deteriorating patients on a general medical ward prior and after referral to the hospitals' Acute Care Team (ACT). Further, to provide evidence that the Philips IGS assists to increase the efficiency of a hospital's Early Warning Scoring process (afferent and efferent arm of the escalation system). The introduction of such an intelligent automated system offers a unique opportunity to address the breakdown in the chain of prevention by strengthening the reliability of calls-for-help to responders through a technical solution with the potential for a more timely escalation where appropriate. In this study the hospital's Standard of Care protocol for the monitoring of vital signs (including timing, vital signs collected and escalation instructions) will be implemented in a commercially available intelligent automatic monitoring and notification system. No investigational procedures or devices are associated with this protocol.

Registry
clinicaltrials.gov
Start Date
October 2012
End Date
February 2016
Last Updated
10 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • all patients admitted to the study units during the period of data collection

Exclusion Criteria

  • less than 24h on ward

Outcomes

Primary Outcomes

Improvement of outcome for patients after implementing the IGS

Time Frame: 15 months

Does the IGS significantly increase positive outcomes for deteriorating patients after referral to the RRT/ACT as measured by the MAELOR score

Secondary Outcomes

  • Early detection of patient deterioration(15 months)
  • Daily workload for the ward's personnel(15 months)
  • Level of satisfaction(15 months)

Study Sites (1)

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