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Testing a Brain Implant That Detects Seizures in People With Epilepsy

Tests whether a deep brain stimulator can detect seizures in adults with drug-resistant epilepsy.

Plain-language title generated from the registry record
Registry title: Thalamus Seizure Detection With a Deep Brain Stimulator System

Key facts

Where
Rochester, United StatesSee the site

Where in United States

  • Mayo Clinic in RochesterRochester, United StatesTaking people

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Trial details

Who runs it
Mayo Clinic
Trial code
NCT06700356
Record updated
13 July 2026
Original description
The purpose of this study is to determine the feasibility of chronic ambulatory thalamus seizure detection. The sensitivity, specificity, and false alarm rate of thalamus seizure detection will be calculated using recordings from a deep brain stimulation system, assessed relative to concurrent gold-standard video-EEG monitoring collected in the in-patient setting (epilepsy monitoring unit), in 5 patients with drug resistant epilepsy.Read full original descriptionShow less

Seizure Detection With a Deep Brain Stimulation System

The purpose of this study is to determine the feasibility of chronic ambulatory thalamus seizure detection. The sensitivity, specificity, and false alarm rate of thalamus seizure detection will be calculated using recordings from a deep brain stimulation system, assessed relative to concurrent gold-standard video-EEG monitoring collected in the in-patient setting (epilepsy monitoring unit), in 5 patients with drug resistant epilepsy.

Inclusion: Participants must meet all of the inclusion criteria to participate in this study:; 18 years of age and older; Implanted with a clinical DBS system for epilepsy with brain recording capabilities (Medtronic Percept™ DBS); Subject or legally authorized representative is able to understand study procedures and to comply with them for the entire length of the study.

Exclusion: Current drug or alcohol use or dependence that, in the opinion of the site investigator, would interfere with adherence to study requirements; Health status or any clinical conditions (e.g., life expectancy, co-existing disease) that, in the opinion of the site investigator, would pose undue risk to undergo epilepsy monitoring unit evaluation for the purpose of seizure characterization; All candidates meeting any of the exclusion criteria at baseline will be excluded from study participation:; Women will verify not pregnant, and if applicable, have urine pregnancy test; Inability or unwillingness of individual or legal guardian/representative to give written informed consent.

ClinicalTrials.gov NCT06700356