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Outcomes and User Acceptance of the IntelliVue Alarm Advisor Software (USA)

NCT03347149 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1336

Last updated 2018-04-10

No results posted yet for this study

Summary

This Clinical Study will be conducted as a comparative study focusing on usability and efficiency by comparing alarm burden pre- and post- implementation of an "Alarm Advisor software".

Conditions

  • Clinical Alarms

Interventions

DEVICE

Alarm Advisor Software

Providing advice on alarm limits as part of routine medical care

Sponsors & Collaborators

  • Yale University

    collaborator OTHER

  • Philips Healthcare

    lead INDUSTRY

Principal Investigators

  • Marjorie Funk, PhD, Professor · Yale School of Nursing

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-08-28
Primary Completion
2018-03-11
Completion
2018-03-11

Countries

  • United States

Study Locations

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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 NCT03347149 on ClinicalTrials.gov