Klinikum Konstanz
Konstanz, Baden-Wurttemberg, 78464, Germany
NCT Number: NCT03182452
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".
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Notify Me18 year and older
All sexes
Observational
Konstanz, Baden-Wurttemberg, 78464, Germany
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Providing advice on alarm limits as part of routine medical care
Time frame: six to eight months
Number of Different Alarms on Intensive Care
Philips Healthcare
Industry
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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