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Clinical Trial Summary

This study is designed as a prospective, non-randomized, observational clinical study. The study will collect clinical and rrEEG (Ceribell EEG) data when monitoring subjects for delirium subtypes. EEG and clinical data will be collected for the development of future software algorithms to assess the presence and severity of delirium.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04962815
Study type Observational [Patient Registry]
Source Ceribell Inc.
Contact Michelle Hofmann, MSN
Phone 800-436-0826
Email michelle.hofmann@ceribell.com
Status Recruiting
Phase
Start date November 10, 2021
Completion date December 31, 2024

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