EEG Abnormalities in Adult ICU Patients With High Risk of Delirium

Part of paid clinical trials in Nashville, Tennessee.

Sponsor
Ceribell Inc.
Study ID
NCT07485244
Status
Recruiting

Conditions

  • Delirium in the Intensive Care Unit

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Ceribell EEG System — DEVICE
    EEG will be recorded with the Ceribell EEG System, including headband and recorder.

Study Details

The purpose of this study is to assess the prevalence of EEG abnormalities on Ceribell POC EEG in adult medical, surgical, and cardiovascular ICU patients with high risk of delirium

Key Dates

Start date
Apr 16, 2026
Status verified
Apr 2026
Primary completion
Dec 31, 2026
Completion
Sep 30, 2027

Study Design

Enrollment
100 participants (estimated)

Arms

  • Arm: Prospective Ceribell Delirium Monitoring
    Enrolled patients will undergo EEG monitoring with the Ceribell EEG System twice daily for up to 7 days.

Primary Outcome Measure

Prevalence of EEG Abnormalities on the Ceribell EEG System [ Time Frame: Starting baseline through study completion, up to 1 year. ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Vanderbilt University Medical CenterNashvilleTennessee37232
Anya Harden
615-936-7355
Wesley Ely, MD, MPH (PRINCIPAL_INVESTIGATOR)

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