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

NCT02973243 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 446

Last updated 2017-04-12

No results posted yet for this study

Summary

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

Conditions

Interventions

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.

Sponsors & Collaborators

  • Philips Healthcare

    lead INDUSTRY

Principal Investigators

  • Christian P Subbe, MD · Ysbyty Gwynedd Hospital

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-10-05
Primary Completion
2017-02-28
Completion
2017-02-28

Countries

  • United Kingdom

Study Locations

More Related Trials

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 NCT02973243 on ClinicalTrials.gov