Do brain monitors fool seizure kids? study aims to find out
NCT ID NCT07585643
First seen Jun 25, 2026 · Last updated Jul 17, 2026 · Updated 2 times
Summary
This study will check if two common brain monitors used during anesthesia (BIS and Sedline) give accurate readings in children with severe seizure disorders. Researchers will compare these monitors to a standard EEG in 40 children under 16. The goal is to make anesthesia safer for these kids.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this study could help doctors better monitor anesthesia depth in children with seizure disorders, improving safety during surgery.
- What could go wrong
- This is a small, early observational study (40 children) that only measures brain activity while awake. It does not test any treatment or guarantee better outcomes.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 40 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Sep 2029
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
20 eligible patients identified by the neurology department at Perth Children's Hospital and 20 eligible patients identified by the neurology department at Hospital das Clinicas HCFMUSP, Faculdade de Medicina, will be approached for the study.
- Ages
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0 to 15 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Children (\<16 years old) with a confirmed diagnosis of early onset EE or DEE due to any cause (prior to age 2 years). Exclusion Criteria: * Language barriers impeding data collection * Department for Child Protection and Family Support is involved in the care of the child.
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Get notified about this study
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
2 sites in 2 countries. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Hospital das Clinicas, São Paulo, Sao Paulo
São Paulo, Brazil
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Perth Children's Hospital
Perth, Western Australia, 6909, Australia
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Other studies related to the condition(s) this trial covers.
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- New study aims to map rare childhood brain disorder
- New gene test could unlock mysteries of severe epilepsy in kids
- Gene testing may personalize seizure care for infants
- Epilepsy drug study for kids halted early: what we know
- New program aims to ease burden on families of kids with rare diseases