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NOT YET RECRUITING
NCT07449416
NA

Ceribell Delirium Monitor Outcomes Pilot Study

Sponsor: Ceribell Inc.

View on ClinicalTrials.gov

Summary

This pilot study is designed as a pre- and post-delirium monitor cohort study, with a prospective intervention cohort and a retrospective control cohort.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

100

Start Date

2026-03-15

Completion Date

2026-12

Last Updated

2026-03-04

Healthy Volunteers

No

Interventions

DEVICE

Ceribell Delirium Monitoring System

The Ceribell Delirium Monitor provides an assessment of delirium every 15 minutes during each EEG recording and provides a trend graph depicting the output of the algorithm. If delirium is detected, a CAM-ICU assessment will be performed to confirm the presence of delirium. The patient's care team will use the additional data provided by the Ceribell Delirium Monitor to inform decisions regarding alterations in the patient's delirium management.

Locations (1)

University of California Irvine

Irvine, California, United States