Using Rapid-Response EEG to Diagnose Seizures in Children

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to compare the speed of obtaining EEG results using the Ceribell® Rapid Response EEG device against the conventional continuous EEG method in pediatric patients suspected of having status epilepticus. Conducted at a single urban academic pediatric hospital, the study involves a retrospective chart review of patients who underwent either EEG modality within 24 hours of admission to the pediatric ICU. The goal is to determine how much faster the rapid response EEG can provide diagnostic information, which is critical for timely treatment. The study is approved by the Institutional Review Board and focuses on patients with neurological diagnoses and diminished consciousness.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* all patients with suspected status epilepticus as determined by the treating team in the pediatric ER or ICU

Exclusion Criteria:

* none

Where it's running

• Children's Hospital at Montefiore
  The Bronx, New York, United States Recruiting

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.