Low-intensity Focused Ultrasound and Autonomic Response
Enrolling by invitation · Not applicable · Has a placebo group
Conditions studied: Autonomic Dysfunction
In brief
Studying the effects of Low Intensity Focused Ultrasound (LIFU) to the dorsal posterior insula (dPI) and dorsal anterior cingulate cortex (dACC) on autonomic control using a test to probe the autonomic system. A cold pressor task will be performed pre and post LIFU application. Physiologic recordings will be recorded throughout.
Key facts
- Study ID
- NCT05834829
- Run by
- Virginia Polytechnic Institute and State University
- People needed
- 80
- Starts
- 2024-02-22
- Expected to finish
- 2027-12-30
- Last updated by the study team
- 2026-06-08
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Does not meet exclusion criteria.
You may not qualify if…
- The exclusion criteria below are regularly implemented in MRI, CT, and EEG experiments for the safety of the subjects and for data quality assurance.
- Claustrophobia (scanning environment may be uncomfortable).
- Contraindications to MRI: including pacemaker, aneurysm clips, neurostimulators, cochlear implants, metal in eyes, steel worker, or other implants.
- Contraindications to CT: pregnancy
- Active medical disorder or treatment with potential central nervous system (CNS) effects (e.g. Alzheimer's) -
- History of neurologic disorder. (e.g. Parkinson's, Epilepsy, or Essential Tremor)
- History of head injury resulting in loss of consciousness for >10 minutes.
- History of alcohol or drug dependence (through self-report).
- History of cardiac disease
- A current or prior use of any cardiac medication (e.g. beta blockers or other anti-arrhythmics)
- A history of diabetes mellitus or use of diabetic medications (e.g. metformin).
Where it is running
- Fralin Biomedical Research Institute at VTC — Roanoke, Virginia, United States
Full record on ClinicalTrials.gov
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