Brain zapping trial maps current paths in epilepsy patients
NCT ID NCT02263274
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study used 30 epilepsy patients who already had electrodes implanted in their brains for surgery planning. Researchers applied a mild electrical stimulation called tDCS and measured exactly how the current spread. The goal was to improve computer models that predict where the electricity goes, which could help design better brain stimulation treatments in the future.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Transcranial Direct Current Stimulation (tDCS)
- What this could lead to
- If successful, this could lead to more precise tDCS targeting for brain stimulation therapies in conditions like depression or epilepsy.
- What could go wrong
- This is a small, early-stage measurement study, not a treatment trial. The stimulation levels are very low and not expected to change brain function, so direct patient benefits are unlikely.
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
-
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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30 people
The number who actually took part.
- Started
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Nov 2013
- Finished
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Jan 2026
- 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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18 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: Subjects for this study will be recruited from patients undergoing routine intracranial electrode placement as part of the evaluation for surgical treatment of medically refractory epilepsy. Inclusion criteria include: 1. Age ≥ 18 years 2. Placement of intracranial electrode arrays (grid, strip and or depth electrodes) for seizure focus localization and/or mapping of eloquent cortex 3. Able to provide written informed consent 4. English-speaking patients only Exclusion Criteria: 1. Cognitive impairment (Intelligence Quotient \<70) 2. Facial or forehead skin breakdown that would interfere with surface electrode placement 3. Contraindication to MRI 4. Known adhesive allergy 5. Space occupying intracranial pathology including brain tumor, ateriovenous malformation, cavernous malformation, prior surgical resection or significant encephalomalcia that would create unknown tissue inhomogeneity that cannot be accurately modeled. 6. Subjects who have had an electrographic or clinical seizure within one hour prior to the stimulation procedure
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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.
Contacts and locations
Locations
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Neurology
New York, New York, 11106, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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