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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT04266041
Other study ID # D18111 30813
Secondary ID
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date February 9, 2018
Est. completion date March 9, 2028

Study information

Verified date July 2023
Source Dartmouth-Hitchcock Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the study is to use a new method of high-density electroencephalogram (HD-EEG) recording to map brain areas important for movement, sensation, language, emotion, and cognition.


Description:

This study will measure brain waves using high-density EEG. Participants will be asked wear a cap with electrodes attached to it. During the recording, participants may be asked to rest, sleep, or complete a task. The tasks involve viewing pictures, answering questions, speaking, or moving an arm or leg. Recordings generally last between 60-120 minutes.*


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 100
Est. completion date March 9, 2028
Est. primary completion date February 9, 2028
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Able to perform the tasks - Able to give own consent Exclusion Criteria: - Any neurologic or psychiatric diagnosis such as stroke, tumor, or psychosis judged to interfere with high-density EEG.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
High-density electroencephalogram (HD-EEG)
This study will focus on obtaining a special type of high-density scalp electroencephalography (HD-EEG) recordings in patients with neurological disorders (i.e., epilepsy, brain tumor, stroke, etc.) and appropriately matched controls. HD-EEG is a scalp EEG which uses up to 256 channels compared to the standard 21 channels used for routine clinical applications. The reason for using more channels to record is for more precise localization of epileptogenic foci and/or more precise mapping of brain functions. This type of EEG requires the use of patient's own MRI scan to precisely localize activity. Therefore, all patients and controls getting an HD-EEG will require a structural MRI scan.

Locations

Country Name City State
United States Dartmouth-Hitchcock Medical Center Lebanon New Hampshire

Sponsors (1)

Lead Sponsor Collaborator
Dartmouth-Hitchcock Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Localize brain functions in patients and healthy controls Localize brain functions using high-density EEG recordings 60 - 90 minutes
Secondary Localize brain areas involved in language Localize brain areas involved in language using high-density EEG recordings 60 - 90 minutes
Secondary Localize brain areas involved in movement Localize brain areas involved in movement using high-density EEG recordings 60 - 90 minutes
Secondary Localize brain areas involved in sensation Localize brain areas involved in sensation using high-density EEG recordings 60 - 90 minutes
Secondary Localize brain areas involved in emotion Localize brain areas involved in emotion using high-density EEG recordings 60 - 90 minutes
Secondary Localize brain areas involved in memory Localize brain areas involved in memory using high-density EEG recordings 60 - 90 minutes
Secondary Localize brain areas associated with lesions Localize brain areas associated with lesions using high-density EEG recordings 60 - 90 minutes
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