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Clinical Trial Summary

Multi-center observational trial with study device blinded in order to assess in parallel standard monitoring and intervention practices related to management of respiratory compromise in the post-anaesthesia care unit (PACU)


Clinical Trial Description

All Study device information is blinded to medical staff but the Study Coordinator will have full access to device measurements, alarms, notification and events via a local Wi-Fi hub sent to a portable tablet. The tablet Case Report Form (CRF) will allow all observation be inserted with a time stamp on the electronic device data. In addition, all electronic data will be collected from the bedside monitor. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02707003
Study type Observational
Source Medtronic - MITG
Contact
Status Completed
Phase
Start date February 2016
Completion date June 15, 2018

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