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Ceribell Delirium Data Collection Study

Who can join

Ages 18 and older · All sexes

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.

About the study

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.

What is being tested

• Electroencephalogram (EEG) Test (device)

Sponsor: Ceribell Inc. · Participants: 200 · Started: Nov 10, 2021

Contact the study team

• Michelle Hofmann, MSN · Phone: 800-436-0826
• Jessy Dorn, PhD · Phone: 800-436-0826

Official record on ClinicalTrials.gov — NCT04962815

Locations in the U.S.

Conditions

• Delirium

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.