NCT04962815Recruiting
Ceribell Delirium Data Collection Study
Ceribell Inc.
Start Date
11/10/2021
Completion Date
4/1/2026
Summary
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
Age Range: 18 years to No maximum
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.
Interventions
DEVICE
Electroencephalogram (EEG) Test
Conditions
Delirium
Locations
Stanford University
Stanford, California 94305
United States
Naples Community Hospital
Naples, Florida 34102
United States
University of Iowa Hospitals & Clinics
Iowa City, Iowa 52242
United States
Mercy
St Louis, Missouri 63141
United States
Cooper Health
Camden, New Jersey 08103
United States
UNC Health Rex
Raleigh, North Carolina 27607
United States
University of Pittsburgh
Pittsburgh, Pennsylvania 15213
United States