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Clinical Trial Summary

An observational study to assess the BIS reported level of sedation of patients with traumatic brain injury in the ICU.


Clinical Trial Description

Patients admitted to Aberdeen ICU with severe traumatic brain injury will have a BIS electrode placed and observed for 24 hours. The study team will be blinded to the result, so not to influence treatment. All clinical care is at the discretion of the clinical team. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03575169
Study type Observational
Source University of Aberdeen
Contact
Status Completed
Phase
Start date July 1, 2019
Completion date December 31, 2022

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