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Clinical Trial Summary

This study is designed as a prospective, non-randomized, observational, multicenter clinical trial. The primary aim of this study is to observe if the use of the rapid responds electroencephalography (EEG) system impacts physician decision making. Secondary aims include exploring the safety and performance information of the Ceribell EEG system compared to conventional EEG system. The study will recruit physicians (Faculty physicians and Trainees) at up to five institutions and examine the impact of rapid response EEG when providing care to patients in whom EEG recording has been ordered for clinical reasons.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03534258
Study type Observational
Source Ceribell Inc.
Contact
Status Completed
Phase
Start date April 30, 2018
Completion date July 31, 2019

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