Ceribell Delirium Data Collection Study

Recruiting Observational Study
Delirium
No Study Drug Researchers observe your health over time — no experimental treatment is given.
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Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
200 (estimated)
Sponsor
Ceribell Inc. · Industry
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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.

Trial Locations
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Eligibility Criteria
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 syste…
Contacts

Michelle Hofmann, MSN

800-436-0826

michelle.hofmann@ceribell.com

CONTACT

Jessy Dorn, PhD

800-436-0826

jessy.dorn@ceribell.com

CONTACT