Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT05529264

Human Intracranial Electrophysiology

Led by Dartmouth-Hitchcock Medical Center · Updated on 2026-01-15

175

Participants Needed

1

Research Sites

497 weeks

Total Duration

On this page

Sponsors

D

Dartmouth-Hitchcock Medical Center

Lead Sponsor

D

Dartmouth College

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study will enroll patients with epilepsy who are being evaluated for epilepsy surgery and have electrodes implanted in the brain and/or have electrodes on the scalp. Additionally, this study will recruit normal and online controls (participants who do not have epilepsy). Participants will be asked to participate in 1 to 2 (30-90 minutes) daily sessions designed to test aspects of human cognition such as memory, speech, language, feeling, movement, attention, sound perception, and emotions. Generally, this will involve working on a computer, looking at pictures or watching videos, and answering questions. Additionally, participants may be asked to be hooked up to additional equipment such as eye tracker, electrical stimulator, heart rate monitor, sweat monitor or other non-invasive equipment. The overall aim of this study is to use human intracranial electrophysiology (the recording of the electrical activity of the human brain) to study localization and function of the human brain.

CONDITIONS

Official Title

Human Intracranial Electrophysiology

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Must be 18 years or older with no upper age limit
  • Patients with intracranial EEG must have refractory epilepsy and be undergoing intracranial EEG recording for clinical reasons
  • Patients with scalp EEG must have a probable diagnosis of epilepsy
  • Normal control participants must be able to provide informed consent for themselves
Not Eligible

You will not qualify if you...

  • Having additional neurological conditions such as stroke or dementia
  • Having psychiatric conditions like active psychosis or suicidal thoughts that make participation inappropriate
  • Unable to provide informed consent due to reasons like being encephalopathic or currently experiencing a seizure
  • Normal controls deemed not appropriate for the study population

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Dartmouth-Hitchcock Medical Center

Lebanon, New Hampshire, United States, 03776

Actively Recruiting

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Research Team

K

Krzysztof A Bujarski, MD

CONTACT

G

Gina Kersey

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

4

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