Mapping LIFU Responses Using iEEG Recordings

Enrolling by invitation · Not applicable

Conditions studied: Low Intensity Focussed Ultrasound, Electrodes, Implanted

In brief

The current study presents a unique opportunity to measure the immediate neural responses to brief, non-therapeutic transcranial low-intensity focused ultrasound (LIFU) pulses using intracranial electrodes. By recording time-locked signals in local and distant brain regions we can characterize circuit connectivity in real-time. We will use adult patients undergoing intracranial electrophysiological monitoring in an inpatient setting as our targeted population.

Key facts

Study ID

NCT07518927

Run by

University of Pennsylvania

People needed

30

Starts

2026-03-04

Expected to finish

2031-03-04

Last updated by the study team

2026-04-09

Who can join

Age: 21 and older, up to 75. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients who received (or are scheduled to receive) intracranial electrode implantation surgery as part of standard clinical care or as participation in an ongoing research study for the treatment of epilepsy and/or neuropsychiatric conditions at Pennsylvania Hospital (PAH) or Hospital of the University of Pennsylvania (HUP).
• Adult patients, 21 to 75 years of age
• Patients considered to be in a stable medical condition, in the opinion of the PI
• Patients who are able to demonstrate comprehension of instructions in the English language, in the opinion of the PI
• Patients who are able to provide informed consent and fully comply with all study requirements, in the opinion of the PI

You may not qualify if…

• Patients with chronic alcohol abuse history
• Patients with additional implanted devices, such as an aneurysm clip, large cranial plates or mesh that may intersect with ultrasonic beam path
• Open scalp wounds, infection or dermatologic condition that preclude safe placement of ultrasound transducer
• Intracranial mass lesion with significant mass effect near intended beam path
• Patients who are pregnant at the time of screening or patients who get pregnant during the course of the study
• Patients with any past or present medical condition, disease, disorder, or injury that, in the opinion of the PI, may reduce or hinder the participant's ability to fully comply with all study requirements or may impact, compromise, or affect the integrity of the data or the results of the study

Where it is running

• University of Pennsylvania — Philadelphia, Pennsylvania, United States

Full record on ClinicalTrials.gov

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