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The study was approved by the regional ethics committee of Friuli Venezia Giulia, Italy (CEUR-2016-Sper-066-ASUIUD). Each patient or legally authorized representative must provide written informed consent for the study procedures.
An observational analysis was conducted to assess the feasibility of the trial. This observational study enrolled patients admitted to the ICU of the Department of Anaesthesia and Intensive Care – Azienda Sanitaria Universitaria Integrata di Udine (Italy).
JMIR Res Protoc 2017;6(5):e78
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