NaviFUS™ System Neuromodulating Treatment for Patients With Drug Resistant Epilepsy
Drug Resistant Epilepsy
About this trial
This is an interventional treatment trial for Drug Resistant Epilepsy
Eligibility Criteria
Inclusion Criteria:
- Male or female patients aged ≥20 years old.
- Patients with drug-resistant epilepsy (defined as at least 3 ASM failed) and 1-4 ASM at the time of study entry.
- An epileptogenic foci is determined by comprehensive presurgical evaluation
- Seizure number is countable and had been recorded at least 6 times within 2-month in medical history before screening period.
- Seizure number had been recorded at least 3 times within 28-day screening period.
- Willing and able to sign written informed consent and be able to comply with the study protocol during the study period.
Exclusion Criteria:
- Patients with concurrent active psychiatric or mood disorders that in the opinion of the investigator would interfere with participation in the study.
- Presence of pacemaker, implantable cardioverter-defibrillator (ICD), permanent medication pumps, cochlear implants, or deep brain stimulation (DBS)
- The skull bone area traversed by the sonication pathway is covered by scars, scalp disorders (e.g., eczema), or atrophy of the scalp.
- Clips or other metallic implanted objects in the FUS exposure path, except shunts.
Abnormal coagulation profile:
- Platelet (PLT) < 100,000/μL.
- prothrombin time (PT) >14 sec.
- activated partial thromboplastin time (APTT) >36 sec.
- and international normalized ratio (INR) > 1.3.
- Pregnant or breast-feeding women.
- Coexisting medical problems of sufficient severity to limit compliance with the study.
- Known sensitivity/allergy to Magnetic Resonance Imaging (MRI) contrast agents or any of its components.
- Use of any recreational drugs or history of drug addiction or known history of substance or alcohol abuse.
- Patients have received an investigational drug or an investigational device within 4 weeks prior to the study.
- Any other condition that, in the investigator's judgment, might affect study endpoints or might increase the risk to the patients or decrease the chance of obtaining satisfactory data needed to achieve the objectives of the study.
- Any ASM treatment change during the baseline (screening period)
- Vagus nerve stimulation (VNS) dosing changes within 2 months before baseline (screening period).
- Radiofrequency thermocoagulation (RFTC) within 2 months before baseline (screening period).
- Any other condition that, in the investigator's judgment, patient not applicable to participate this study.
Sites / Locations
- Taipei Veterans General HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Sham Comparator
FUS treatment
Sham treatment
FUS treatment will be conducted with following exposure parameters: intracranial spatial-peak temporal-average intensity (ISPTA) ceiling level: 2.8 W/cm2 (the focused ultrasound intensity in brain area considering transcranial attenuation), burst length: 3 ms, duration: three consecutive 5-minute FUS exposures with two 5-minute intermission intervals. The FUS exposure area will be the epileptogenic focus which is individually different and determined by standard clinical practice previously.
Sham treatment is to mimic the FUS treatment procedure but without any energy. The ISPTA will be 0 W/cm2, duration: three repeating 5-minute sham exposures with two 5-minute intermission intervals.