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Acute Recording of Stereotyped High-Frequency Oscillations

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Mayo Clinic

Status

Enrolling

Conditions

Epilepsy

Treatments

Device: Brain Interchange System

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT05439655
23-008859
1UH3NS117944-01A1 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

Overall, this study will investigate the functional utility of stereotyped HFOs by capturing them with a new implantable system (Brain Interchange - BIC of CorTec), which can sample neural data at higher rates >=1kHz and deliver targeted electrical stimulation to achieve seizure control. In contrast to current closed-loop systems (RNS), which wait for the seizure to start before delivering stimulation, the BIC system will monitor the spatial topography and rate of stereotyped HFOs and deliver targeted stimulation to these HFO generating areas to prevent seizures from occurring. If the outcomes of our research in an acute setting become successful, the investigators will execute a clinical trial and run the developed methods with the implantable BIC system in a chronic ambulatory setting.

Full description

High-frequency oscillations (HFOs) of intracranial EEG (iEEG) have the potential to identify the surgical resection area/seizure onset zone (SOZ) in patients with drug-resistant epilepsy. However, multiple reports indicate that HFOs can be generated not only by epileptic cerebral tissue but also by non-epileptic sites often including eloquent regions such as motor, visual, and language cortices. In this project, the initial evidence of a recurrent waveform pattern is presented that may be sufficient to distinguish pathological HFOs from physiological ones. Specifically, the investigators show that the SOZ repeatedly generates sets of stereotypical HFOs with similar waveform morphology whereas the events recorded from out of SOZ were irregular. This morphological pattern served as a robust neurobiomarker to isolate SOZ from other brain areas in multiple patients consistently. While these promising preliminary results are in place, the functional utility of stereotyped HFOs in a closed-loop seizure control system remains unknown. As of today, not much is known whether the stereotyped HFOs generated by the SOZ can be detected with an implantable system. If this can be achieved, then HFOs can be strategically translated as a neurobiomarker into closed-loop seizure control applications. The investigators hypothesize that pathologic stereotyped HFOs can be captured with the implantable Brain Interchange (BIC) system of CorTec and spatial topography of these events can be utilized by the implantable system to deliver targeted electrical stimulation to achieve seizure control. Using an acute setup within the epilepsy monitoring unit (EMU), this project will investigate the feasibility of capturing stereotyped HFO events using the new BIC system and compare the detection results to those obtained with the commercially available amplifier (Aim-1). If the first phase (Aim-1) of the study becomes successful, later in the second phase (Aim-2), once again in the EMU, the investigators will deliver targeted electrical stimulation to those brain sites associated with stereotyped HFOs using the BIC.

During the entire study, the BIC system will not be implanted but used externally to assess the neural data through externalized electrodes and then deliver closed-loop stimulation. If the outcomes of the research in an acute setting become successful, the investigators will execute a clinical trial and run our methods with the implanted BIC system in a chronic ambulatory setting.

Enrollment

12 estimated patients

Sex

All

Ages

3 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients with medically refractory epilepsy, who have been deemed appropriate candidates for intracranial EEG monitoring
  • Adult men and women (18≤ age <70 years)
  • children (3≤ age <18 years)
  • includes women and minorities

Exclusion criteria

  • Subjects will be excluded if their condition makes them unable to continue with recordings.

Trial design

Primary purpose

Device Feasibility

Allocation

N/A

Interventional model

Sequential Assignment

Masking

None (Open label)

12 participants in 1 patient group

Epilepsy
Experimental group
Description:
patients with drug resistant epilepsy undergoing a surgical evaluation in the epilepsy monitoring unit
Treatment:
Device: Brain Interchange System

Trial contacts and locations

2

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Central trial contact

Gregory A Worrell, M.D., Ph.D.; Nuri F Ince, Ph.D.

Data sourced from clinicaltrials.gov

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