Ceribell Delirium Data Collection Study
ConditionDelirium
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCeribell Inc.
About this trial
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.
Eligibility criteria
Qualifiers
Age is 18 years or older
Admitted to the Intensive Care Unit (ICU)
Subject must be fluent in the language in which the delirium assessment is performed
Disqualifiers
None
Trial design
Treatments tested in this trial
- Electroencephalogram (EEG) Test
Treatment groups
No treatment groups listed
Sponsors and collaborators
Source ClinicalTrials.gov