New EEG method aims to catch hidden seizures in tiny ICU patients
NCT ID NCT06726408
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study tests a new brain monitoring method for children under 2 in intensive care. It uses 10 electrodes and special software to detect seizures that are otherwise invisible. The goal is to see if this approach is more accurate than current simpler methods, helping doctors treat seizures faster and improve long-term brain health.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- neuromonitoring with 10 electrodes and quantitative EEG software
- What this could lead to
- If successful, this could lead to a more accurate, bedside-friendly way to detect hidden seizures in young children in intensive care, improving their neurological outcomes.
- What could go wrong
- This is an early diagnostic study with 120 participants, so results may not apply to all hospitals or age groups. The new method may not be more accurate than current simplified techniques.
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 120 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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Sep 2027
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
Patients younger than 2 years old hospitalized in the intensive care unit with an indication for neuromonitoring
- Ages
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Up to 24 months
- 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 : * Patients younger than 2 years old hospitalized in the intensive care unit with an indication for neuromonitoring. The same patient may be included multiple times. * Written non-opposition from legal representatives. * Patients affiliated with or beneficiaries of a social security or similar scheme (CMU). Exclusion Criteria : * Parents who do not understand French. * Inability to set up monitoring equipment (neurosurgery preventing access to electrode placement sites). * Corrected age \< 37 weeks of gestation (GA) for preterm infants.
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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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CHU de Nantes
RECRUITINGNantes, 44093, France
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