Does Use of Rapid Response EEG Impact Clinical Decision Making (DECIDE)

Ceribell

Status: Completed

Conditions: Seizures; Nonconvulsive Status Epilepticus

Treatments: Device: Ceribell Rapid Response EEG, Survey

Study type: Observational

Funder types: Industry

Identifiers

NCT03534258

1825

Details and patient eligibility

About

This study is designed as a prospective, non-randomized, observational, multicenter clinical trial. The primary aim of this study is to observe if the use of the rapid responds electroencephalography (EEG) system impacts physician decision making. Secondary aims include exploring the safety and performance information of the Ceribell EEG system compared to conventional EEG system. The study will recruit physicians (Faculty physicians and Trainees) at up to five institutions and examine the impact of rapid response EEG when providing care to patients in whom EEG recording has been ordered for clinical reasons.

Enrollment: 164 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients undergoing clinically ordered EEGs.

Exclusion criteria

• None