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tFUS Induced Transient Scotoma for Individual Dosing

Medical University of South Carolina · NCT06426498

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 18–70 · All sexes
Healthy volunteers
Accepted
Study type
Interventional · Not applicable
Target enrollment
30
US sites recruiting
1
Study start
June 20, 2024
Record last updated
May 29, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

The purposes of this research study is to

  • Develop a technique of transcranial Focused Ultrasound Stimulation (tFUS) where meaningful effects on the brain can be easily measured.
  • Use this technique to measure threshold for effective tFUS in individuals.
  • Determine whether disruption of conscious visual detection, versus non-conscious visually-guided behavior have different thresholds for disruption with tFUS.

Being studied: Brainsonix Bx Pulsar machine tFUS

Conditions: Healthy

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

  • Male or female
  • Age 18-70
  • Normal or corrected-to normal vision and hearing
  • No neurological or psychological illness

Exclusion Criteria

  • Diagnosis of any depressive or anxiety disorder
  • Diagnosis of schizophrenia or bipolar disorder
  • Current use of any non-prescribed psychoactive medications or drugs
  • Contraindication to enter the MRI environment.
  • Pregnancy (or suspected/possible pregnancy or plan to become pregnant in the short term).
  • Urine Pregnancy Test: If the subject is a woman of childbearing potential and /or a man capable of fathering a child before, during, and/or after participation precaution should be taken. Examples of acceptable methods of birth control for participants involved in the study include: birth control pills, patch, IUD, condom, sponge, diaphragm with spermicide, or avoiding sexual activity that could cause the subject to become pregnant.
  • Inability to adhere to treatment schedule.
  • Initiation of new antidepressant treatment at the time of study randomization.

NOTE: There will be no exclusion based upon gender or minority status. We anticipate that at least 50% of the participants will be women. The percentage of minority participants is expected to be at least 5%. We will make vigorous attempts to increase this number by posting advertisement flyers in minority communities.

Children, prisoners, and institutionalized individuals will not be recruited, because they are beyond the scope of the objectives. Moreover, we will emphasize that participation in this study is completely voluntary. Recruitment of women and minorities has been addressed above. Non-English speaking subjects will not be recruited because they may not be able to understand instructions, which could undermine the validity of the results.

Recruiting US locations

  • Medical University of South Carolina Brain Stimulation Division

    Charleston, SC 29425

    Site contact: Mark S George, MD · 843-876-5142 · georgem@musc.edu

Study contacts (from the official record)

  • Bridgette Holland · 843 638 7517 · hollanbr@musc.edu
  • Mark S George, MD · 843 876 5142 · georgem@musc.edu
tFUS Induced Transient Scotoma for Individual Dosing (NCT06426498) | Bored Studies