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NCT02973243 Clinical Trial

The Vital Signs to Identify, Target, and Assess Level (VITAL) Care Study III

Myocardial Infarction Clinical Trial

Official title:
The Vital Signs to Identify, Target, and Assess Level (VITAL) Care Study III

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02973243
Other study ID # YGB-816-VITALIII
Secondary ID
Status Completed
Phase N/A
First received November 22, 2016
Last updated April 11, 2017
Start date October 5, 2016
Est. completion date February 28, 2017

Study information
Verified date April 2017
Source Philips Healthcare
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To evaluate the effect of automated recording on frequency of recorded scores, number of automated notifications and serious events.

Description:

The frequency of EWS scores, number of automated notifications and serious events performed on a general ward is contingent on the quality and frequency of vital signs measurement like respiratory rate. This is due to the EWS escalation schemes of hospitals with an acute intervention team. Obtained sub-score trigger levels of vital signs contribute to higher and more frequent scoring.

We examine the influence of different respiration rate sensor concepts and measurements on scoring (NEWS and CREWS) and workflow in a typical UK gastroenterology and respiratory ward.

Recruitment information / eligibility
Status Completed
Enrollment 446
Est. completion date February 28, 2017
Est. primary completion date February 28, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- patients admitted to the study units during the period of data collection

Exclusion Criteria:

- palliative patients

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• Automatic RR Measurement
Different newly developed respiration rate sensors are applied at the bedside during the intervention phase which send data to the IntelliVue Guardian System.

Locations
Country Name City State
United Kingdom Ysbyty Gwynedd Hospital Bangor

Sponsors (1)
Lead Sponsor Collaborator
Philips Healthcare

Country where clinical trial is conducted

United Kingdom, 

Outcome
Type Measure Description Time frame Safety issue
Primary Number of NEWS Scores 8-12 Weeks
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