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Flexible High-Density Brain Electrodes to Guide Epilepsy Surgery in Focal Epilepsy

Tests a flexible brain-surface electrode during surgery for people with focal epilepsy.

Plain-language title generated from the registry record
Registry title: High-density Flexible μECoG for Epilepsy Surgery - A Single-Arm ECT

Key facts

Where
Beijing, ChinaSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 3 and 60 years old?

Source: NCT07656857, who can take part

Where in China

  • Beijing Tiantan HospitalBeijing, ChinaTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Beijing Tiantan Hospital
Trial code
NCT07656857
Record updated
13 August 2026
Original description
What's the clinical value of high-density flexible microelectrocorticography (μECoG) for guiding the resection of epileptogenic zone (EZ) in epilepsy surgery?Read full original descriptionShow less

Precision Resection of the Epileptogenic Zone Using Intraoperative Submillimeter Micro-Electrocorticography (Epi-PRECISE): A Single-Arm Trial With an External Historical Control Cohort

What's the clinical value of high-density flexible microelectrocorticography (μECoG) for guiding the resection of epileptogenic zone (EZ) in epilepsy surgery?

Inclusion: Age 3 to 60 years; Diagnosis of drug-resistant epilepsy, defined as persistent seizures despite treatment with two or more appropriately selected, adequately dosed and adequately tried antiseizure medications; Diagnosis of focal epilepsy after standard presurgical evaluation and considered suitable for resective epilepsy surgery; Preoperative cognitive or developmental status sufficient to participate in study assessments, as judged by the investigator and assessed using age-appropriate validated instruments. For participants aged 3 to 6 years, developmental status must be within the normal range according to the Griffiths Mental Development Scales. For participants aged 6 to 16 years, cognitive function must be within the normal range according to the Wechsler Intelligence Scale for Children. For participants older than 16 years, a Mini-Mental State Examination score of 24 or higher will be required; Written informed consent provided by the participant or, when applicable, by a legal guardian.

Exclusion: History of any previous neurosurgical craniotomy before epilepsy surgery; Contraindication to surgery; Suspected mesial temporal lobe epilepsy after multidisciplinary presurgical evaluation; Severe psychiatric, cognitive, or psychological disorder that prevents participation in the study or completion of follow-up.

ClinicalTrials.gov NCT07656857