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.
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Change in physicians' diagnosis decision
Timeframe: through study completion, an average of 1 year
Change in physicians' diagnosis confidence
Timeframe: through study completion, an average of 1 year
Change in physicians' treatment decision
Timeframe: through study completion, an average of 1 year
Change in physicians' treatment confidence
Timeframe: through study completion, an average of 1 year