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

Trial ID or NCT#

NCT06388707

Status

not recruiting iconNOT RECRUITING

Purpose

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).

Official Title

A Prospective, Open-label, Single-arm, Multi-center, Pilot Study to Evaluate the Safety, Tolerability, and Preliminary Efficacy of Low-intensity Focused Ultrasound Neuromodulation in Patients With Drug-resistant Unilateral or Bilateral Temporal Lobe Epilepsy

Eligibility Criteria

Sexes Eligible for Study: ALL
Accepts Healthy Volunteers: Yes

Investigator(s)

RobertÌýFisher, MD, PhD
RobertÌýFisher, MD, PhD
Epilepsy specialist, Neurophysiologist, Neurologist
The Maslah Saul, MD, Professor and Professor, by courtesy, of Neurosurgery

Contact us to find out if this trial is right for you.

Contact

SPECTRUM
650-725-6648