CompletedNot Applicable

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

United States1,336 participantsStarted 2017-08-28

Plain-language 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".

Who can participate

Age range18 Years

SexALL

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Inclusion Criteria: \- Patients admitted to the intensive care units during the study periods Exclusion Criteria: \- none

What they're measuring

Number of Alarms

Timeframe: 2 month per phase with 2 month washout (6 month overall)

Trial details

NCT IDNCT03347149

SponsorPhilips Healthcare

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2018-03-11

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