Subcortical Arousal In Perceptual Awareness

Overview

About this study

The study is a multi-site study and will be conducted at up to 11 investigative sites in the United States. The study will investigate subcortical arousal circuits in visual perception using techniques with complementary strengths based on promising initial studies.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

The following are the inclusion/exclusion criteria for epilepsy patients with thalamic electrodes age 13 years and up (Aim 1):
Inclusion Criteria:
* normal vision with or without the use of corrective lenses
* normal hearing not needing an assistive hearing device

Exclusion Criteria:
* severe vision impairment even with correction preventing ability to see stimuli (prevents accurate pupil and eye gaze measurements)
* unable to perform the perception task due to cognitive impairment other than due to the participant's epilepsy. All participants must be capable of consenting for themselves.

The following are the inclusion/exclusion criteria for epilepsy patients with thalamic electrodes age 18 years and up (Aim 2):
Inclusion Criteria:

* normal vision with or without the use of corrective lenses
* normal hearing not needing an assistive hearing device
* a female subject must have a negative pregnancy test and if sexually active, must be using a reliable form of birth control for the duration of the trial, be surgically sterile, or be at least two years post-menopausal.

Exclusion Criteria:
* severe vision impairment even with correction preventing ability to see stimuli (prevents accurate pupil and eye gaze measurements)
* unable to perform the perception task due to cognitive impairment other than due to participant's epilepsy. All participants must be capable of consenting for themselves.
* pregnancy

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 8/29/2025. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Jamie VanGompel

Contact us for the latest status

Contact information:

Ana Sanchez

(507) 255-9846

Sanchez.Ana2@mayo.edu

More information

Publications

Publications are currently not available
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CLS-20597444

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