Status:
COMPLETED
eVent in the Human Patient Simulator
Lead Sponsor:
University of British Columbia
Conditions:
Efficacy of the Expert System's Ability to Help Detect Critical Events
Eligibility:
All Genders
Brief Summary
In this study, the investigators are testing the expert system called eVENT. eVENT provides expert advice about the patient's breathing. The investigators have developed and tested a prototype of eVEN...
Detailed Description
The development of new sensors or the intelligent synthesis of existing signals (smart sensors) cannot reliably prevent adverse events unless the investigators assimilate the data produced from these ...
Eligibility Criteria
Inclusion
- Staff anesthesiologist, fellows and 3rd - 5th year residents will be able to participate in this study.
- Subjects willing to provide informed consent.
Exclusion
- Inability/failure to provide informed consent.
- Presence of any of the following conditions oPrevious participation in similar experiment oTaken sedative medication within last 24 hours
- Inability/failure to obtain 75% or above in the post-training quiz on the correct use of the eVent.
- Evaluation will be immediately discontinued at request of subject at any point during the study.
Key Trial Info
Start Date :
December 1 2010
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
June 1 2011
Estimated Enrollment :
36 Patients enrolled
Trial Details
Trial ID
NCT01240317
Start Date
December 1 2010
End Date
June 1 2011
Last Update
June 26 2017
Active Locations (1)
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1
BC Children's Hospital
Vancouver, British Columbia, Canada, V6H 3V4