Ceribell Delirium Data Collection Study
- Conditions
- Delirium
- Registration Number
- NCT04962815
- Lead Sponsor
- Ceribell Inc.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 200
Inclusion Criteria: All must be present<br><br> - Age is 18 years or older<br><br> - Admitted to the Intensive Care Unit (ICU)<br><br> - Subject must be fluent in the language in which the delirium assessment is performed<br><br>Exclusion Criteria: All must be absent<br><br> - Any condition that prevents use of the Ceribell EEG system on the subject for the<br> entire anticipated EEG monitoring period. Examples may include: Craniectomy with<br> missing bone flap in an area where Ceribell EEG electrodes are placed. Expected use<br> of continuous clinical EEG for the entire anticipated monitoring period.
Not provided
Study & Design
- Study Type
- Observational [Patient Registry]
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Perform Confusion Assessment Method for the ICU (CAM-ICU) assessment;Perform Electroencephalogram (EEG) Test
- Secondary Outcome Measures
Name Time Method