Rapid-Response EEG in Children With Suspected Status Epilepticus

Part of paid clinical trials in The Bronx, New York.

Sponsor
Children's Hospital at Montefiore
Study ID
NCT06564662
Status
Recruiting

Conditions

  • Coma
  • Status Epilepticus

Eligibility Criteria

Sex
ALL
Age
2 Years - 18 Years
Healthy Volunteers
Not accepted

Interventions

  • Rapid Response EEG — DEVICE
    The Ceribell(R) Rapid Response EEG is a relatively new device that is becoming standard of care in the adult critical care. In this pediatric study the device will be placed by trained ICU physicians

Study Details

Seizures are common in children (\~350 per 100,000 patients per year) and require immediate medical attention. If the seizure is prolonged (\> 5 minutes) it is called status epilepticus and delayed treatment leads to higher risk in drug resistance and brain injury. The current standard of care for children admitted to the ICU with established or suspected status epilepticus is to start a conventional continuous EEG study that helps diagnosing seizures by typical electro graphic patterns. It takes on average 4 hours to start and another two hours to obtain a reading by epileptologists. This is far beyond the time window of starting an EEG study (60 minutes) as recommended by the neurocritical care society. In adult ICUs, point of care "Rapid Response EEG" are becoming a new standard of care and our ICU adopted this practice in 2020. It can be easily placed by the ICU staff rather than a specifically trained EEG technician but has a lower resolution due to fewer leads (10 vs. 20). The purpose of this study is to determine wether and by how much time RR-EEG yields faster preliminary EEG reports that the previously available conventional EEG (cEEG) and wether the detection of electro graphic seizures is comparable. This is a retrospective cohort study following patients who are admitted to the PICU and are placed on either cEEG or RR-EEG for status epilepticus.

Key Dates

Start date
Dec 9, 2021
Status verified
Aug 2024
Primary completion
Dec 8, 2026
Completion
Dec 8, 2026

Study Design

Enrollment
60 participants (estimated)

Primary Outcome Measure

Time from order of electroencephalogram (EEG) to EEG reading [ Time Frame: up to 24 hours ]

Locations (1)

FacilityCityStateZIPSite coordinators
Children's Hospital at MontefioreThe BronxNew York10467
Michael Miksa, MD, PhD
714-484-5123

Find similar trials in The Bronx, NY

Related Studies