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Clinical Trial 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".


Clinical Trial Description

In a first phase of data collection (pre-implementation) all alarms of an intensive care unit population are recorded.

In an interim period an Alarm Advisor software will be introduced to the unit. In a second phase (post-implementation) the same set of alarm data will be recorded.

The "Alarm Advisor" Software can identify alarms based on criteria set by the medical staff and provide hints to reduce alarms and alarm nuisance (e.g. by proposing adjustments of alarm limits).

The effect of reduction of recurring nuisance alarms through the implementation of the Alarm Advisor shall be evaluated. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03347149
Study type Observational
Source Philips Healthcare
Contact
Status Completed
Phase
Start date August 28, 2017
Completion date March 11, 2018

See also
  Status Clinical Trial Phase
Completed NCT03182452 - Outcomes and User Acceptance of the IntelliVue Alarm Advisor Software (Europe)
Completed NCT02319421 - Reducing the Risk of Alarm Fatigue Through the Use of Focused Management in Safety Huddles N/A
Not yet recruiting NCT06089239 - De-Implementing Fall Prevention Alarms in Hospitals N/A