Ignite Creation Date:
2024-05-05 @ 10:47 PM
Last Modification Date:
2024-10-26 @ 10:24 AM
Study NCT ID:
NCT01197326
Status:
COMPLETED
Last Update Posted:
2016-05-05
First Post:
2010-09-03
Brief Title:
The Prevention of Failure to Rescue Using Early Warning Scoring
Sponsor:
Philips Healthcare
Organization:
Philips Healthcare
Study Overview
Official Title:
The Use of IntelliVue Patient Monitor MP5 Rel G1 for the Prevention of Failure to Rescue Using Early Warning Score
Status:
COMPLETED
Status Verified Date:
2016-04
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
VitalCare
Brief Summary:
The purpose of this study is to assess if compared with standard paper-based systems an automated Early Warning System EWS resident in a spot check patient monitor can help to identify deteriorating patients
Detailed Description:
The purpose of this study is to assess if compared with standard paper-based systems an automated Early Warning System EWS resident in a spot check patient monitor can help to identify patients in the acute care settings but outside of the intensive care unit who may be experiencing physiological instability and who are in need of rapid clinical intervention by a Rapid Response Team RRT Medical Emergency Team MET
The development of such an automated system by offers a unique opportunity to assess its user-friendliness labour-saving effect feasibility and clinical utility Accordingly we plan to conduct a research program aimed at assessing this new approach toward patient monitoring
This study will use the hospitals Standard of Care protocol for the monitoring of vital signs including timing and vital signs collected and a commercially available automatic spot check monitor to collect data No investigational procedures or devices are associated with this protocol
The development of such an automated system by offers a unique opportunity to assess its user-friendliness labour-saving effect feasibility and clinical utility Accordingly we plan to conduct a research program aimed at assessing this new approach toward patient monitoring
This study will use the hospitals Standard of Care protocol for the monitoring of vital signs including timing and vital signs collected and a commercially available automatic spot check monitor to collect data No investigational procedures or devices are associated with this protocol
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None