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Clinical Trials/NCT05200455
NCT05200455
Completed
Not Applicable

Microelectrodes in Epilepsy

Dartmouth-Hitchcock Medical Center1 site in 1 country34 target enrollmentSeptember 18, 2009
ConditionsEpilepsy

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Epilepsy
Sponsor
Dartmouth-Hitchcock Medical Center
Enrollment
34
Locations
1
Primary Endpoint
Feasibility of Microelectrode Technology to Isolate Place Responsive Neurons in the Human Hippocampus as Measured by the Number of Place Responsive Neurons.
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

The purpose of this study is to test microelectrodes in intracranial monitoring to see if they will provide novel information on the epileptic potential of the implanted brain tissue. A secondary objective is to investigate the activity of single neurons during specific cognitive tasks.

Detailed Description

The standard-of-care for medically refractory epilepsy is resective brain surgery. In certain patients, precise localization of the epileptic focus is done using intracranial EEG (iEEG) recording. In this type of EEG recording, electrodes are placed on the brain surface or inserted into the brain through an opening in the skull. In addition to standard electrode recording, this study will use ultra thin microelectrodes. Microelectrodes are only several micrometers thick and are useful because they are able to record the activity of single neurons in isolation. Such recordings have tremendous clinical potential in epilepsy surgery and tremendous research potential in cognitive neuroscience.

Registry
clinicaltrials.gov
Start Date
September 18, 2009
End Date
May 18, 2021
Last Updated
3 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Barbara Jobst

Chair, Department of Neurology

Dartmouth-Hitchcock Medical Center

Eligibility Criteria

Inclusion Criteria

  • 18-65 year old
  • male or female
  • right or left handed
  • medically refractory focal epilepsy requiring intracranial EEG for pre-surgical evaluation deemed medically necessary
  • no contraindications to intracranial electrode study
  • able and willing to participate in research

Exclusion Criteria

  • does not meet the inclusion criteria

Outcomes

Primary Outcomes

Feasibility of Microelectrode Technology to Isolate Place Responsive Neurons in the Human Hippocampus as Measured by the Number of Place Responsive Neurons.

Time Frame: Evaluated for each patient during monitoring period of approximately 2 weeks

With the occipito-temporal implantation approach of implantation of microelectrodes, feasibility will measured by the number of place responsive neurons that could be isolated.

Secondary Outcomes

  • How Precise the Frequencies (Alpha, Beta, Delta, Theta, Gamma, and High-gamma) of Neural Brain Activity Predict the Speed of the Participant at Performing the Cognitive Task (Accuracy Measured in Percentage).(Evaluated for each patient during monitoring period of approximately 2 weeks)

Study Sites (1)

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