Brain recording study aims to personalize epilepsy therapy for kids
NCT ID NCT06453759
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study will record brain activity from deep brain regions (the thalamus) in 30 children already undergoing epilepsy surgery evaluation. Researchers will place extra electrodes to measure how seizures spread and how brain areas connect. The goal is to find better targets for deep brain stimulation, which could help children whose seizures are not controlled by medication.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- additional electrodes placed in the thalamus during standard epilepsy monitoring
- What this could lead to
- If successful, this could lead to personalized deep brain stimulation targets for children with drug-resistant epilepsy, potentially improving seizure control.
- What could go wrong
- This is a small, early-stage observational study (30 participants) that aims to gather data, not test a treatment. It may not lead to immediate clinical benefits, and there is a small risk of bleeding from the extra electrodes.
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.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 30 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2025
- Expected to finish
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Dec 2028
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.
- Ages
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2 to 20 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: 1. All children undergoing SEEG as part of their pre-surgical evaluation at GOSH 2. Participants/parents/legal guardian provide informed consent for inclusion Exclusion Criteria: 1\) Lack of informed consent
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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
1 site. 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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Great Ormond Street Hospital for Children
RECRUITINGLondon, WC1N 3JH, United Kingdom
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Brain implant that fires at seizures tested in teens
- Could a night of soft sounds sharpen the epileptic brain?
- Brain recordings reveal how we keep tabs on others — a window into social navigation
- New brain sensor aims to stop seizures in Drug-Resistant epilepsy
- New pill aims to curb focal seizures in adults
- Virtual tours may help spare memory in epilepsy surgery