Ceribell Delirium Data Collection Study
Purpose
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.
Condition
- Delirium
Eligibility
- Eligible Ages
- Over 18 Years
- Eligible Genders
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
All must be present - 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
Exclusion Criteria
All must be absent - Any condition that prevents use of the Ceribell EEG system on the subject for the entire anticipated EEG monitoring period. Examples may include: Craniectomy with missing bone flap in an area where Ceribell EEG electrodes are placed. Expected use of continuous clinical EEG for the entire anticipated monitoring period.
Study Design
- Phase
- Study Type
- Observational [Patient Registry]
- Observational Model
- Case-Control
- Time Perspective
- Prospective
Recruiting Locations
Pittsburgh, Pennsylvania 15213
More Details
- NCT ID
- NCT04962815
- Status
- Recruiting
- Sponsor
- Ceribell Inc.