New score could spare epilepsy patients from invasive brain probes
NCT ID NCT06138808
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether a simple scoring system, called the 5-SENSE score, can accurately predict where seizures begin in the brain. Researchers will test this in 400 people with hard-to-treat epilepsy who are already scheduled for an invasive brain test called SEEG. If the score works well, it may help some patients avoid this risky procedure in the future.
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 400 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2024
- Expected to finish
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Jun 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
All patients will be prospectively recruited at 20-25 epilepsy centers from North America, Europe, Australia and Asia.
- Ages
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15 years and older
- 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 aged 15 years or older in whom no direct surgical approach can be offered and who are discussed in the multidisciplinary team discussion * availability of complete non-invasive presurgical work-up (including high-resolution MRI according to the in-center epilepsy protocol, video-telemetry with the recording of a minimum of one habitual clinic and EEG seizure, available as original files for review) Exclusion Criteria: * no telemetry/scalp EEG in center * no protocol MRI in center * subdural/GRID electrodes
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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
19 sites in 12 countries. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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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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"Carol Davila" University of Medicine and Pharmacy
Bucharest, Romania
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Alfred Health
Melbourne, Australia
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Christian Doppler University Hospital Paracelsus Medical University Salzburg and Centre for Cognitive Neuroscience Salzburg
Salzburg, 5020, Austria
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Dalhousie Universiry and Hospital
Dalhousie, Nova Scotia, Canada
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Danish Epilepsy Centre, Aarhus Universitets Hospital
Aarhus, 8200, Denmark
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Department of Clinical Neurosciences chez CHUV; Centre Hospitalier Universitaire Vaudois
Lausanne, Switzerland
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Departmet of Neurology, Masaryk University Brno
Brno, Czechia
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Duke University Health System
Durham, North Carolina, 27710, United States
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Epilepsy Centre, University Hospital Freiburg
Freiburg im Breisgau, Germany
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Epilepsy Department University Hospitals of Marseille
Marseille, France
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Grenoble Institute of Neurosciences, Centre Hospitalier Universitaire Grenoble Alpes
Grenoble, France
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Hospital Universitario y Politecnico La Fe
Valencia, Spain
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Mater Health
Brisbane, Australia
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Monash University
Melbourne, Victoria, 3800, Australia
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Northwestern University
Chicago, Illinois, 60611, United States
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Presbyterian-Shadyside Hospital
Pittsburgh, Pennsylvania, 15232, United States
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University School of Medicine Kyoto
Kyoto, 606-8303, Japan
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University of Florida College of Medicine
Gainesville, Florida, 32610, United States
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Wester University
London, Ontario, Canada
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Other studies related to the condition(s) this trial covers.
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