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Study identifier: NCT06388707 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Safety, Tolerability, and Preliminary Efficacy of Low-intensity Focused Ultrasound Neuromodulation in Patients With Drug-resistant Epilepsy

Condition: Drug Resistant Epilepsy · Epilepsy · Seizures, Focal  ·  Sponsor: NaviFUS Corporation

PhasePhase 1/Phase 2
Planned participants8
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This will be a prospective, open-label, single-arm, multi-center, pilot study to evaluate the safety, tolerability, and preliminary efficacy of low-intensity focused ultrasound (LIFU) neuromodulation using NaviFUS System in patients with drug-resistant unilateral or bilateral temporal lobe epilepsy (DR-TLE).

This description comes directly from the study's public registry record.

Talk to the study team

Sheang-Tze Fung, Ph.D.  ·  02-25860560  ·  stfung@navifus.com

Arthur Lung, Ph.D.  ·  arthur.lung@navifus.com

Always discuss trial participation with your own doctor first.

Locations (3)

Stanford University School of MedicinePalo Alto, California, United StatesRecruiting
Brigham and Women's HospitalBoston, Massachusetts, United StatesRecruiting
University of Virginia School of MedicineCharlottesville, Virginia, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06388707