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Trial record 26 of 114 for:    focused ultrasound | Recruiting, Not yet recruiting, Available Studies

MR-Guided Focused Ultrasound in the Treatment of Subcortical Lesional Epilepsy (EP001)

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ClinicalTrials.gov Identifier: NCT02804230
Recruitment Status : Recruiting
First Posted : June 17, 2016
Last Update Posted : January 26, 2018
Sponsor:
Information provided by (Responsible Party):
InSightec

Brief Summary:
The purpose of this study is to evaluate the feasibility, safety, and initial effectiveness of ExAblate thermal ablation of a subcortical focal epileptic target area in the brain of patients suffering from medication-refractory epilepsy, using the ExAblate transcranial system to produce multiple sonications targeted in the lesion of interest. The investigators will establish the feasibility and collect data to establish the basic safety of this type of treatment as the basis for later studies that will evaluate its full clinical efficacy.

Condition or disease Intervention/treatment Phase
Epilepsy, Unspecified, Refractory (Medically) Device: MRgFUS Ablation of Epileptic Foci Not Applicable

Detailed Description:

The purpose of this study is to evaluate the feasibility, safety, and initial effectiveness of ExAblate thermal ablation of a subcortical focal epileptic target area in the brain of patients suffering from medication-refractory epilepsy, using the ExAblate transcranial system to produce multiple sonications targeted in the lesion of interest. The Investigators will establish the feasibility and collect data to establish the basic safety of this type of treatment as the basis for later studies that will evaluate its full clinical efficacy.

The hypotheses tested are that:

  1. MRgFUS treatment of subcortical lesional epilepsy is feasible and safe, with a low risk of adverse effects as evaluated during the follow-up period.
  2. ExAblate treatment of subcortical lesions in patients with subcortical lesional epilepsy reduces the seizure frequency.

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 10 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Feasibility Study to Evaluate Safety and Initial Effectiveness of MR-Guided Focused Ultrasound Ablation Therapy in the Treatment of Subcortical Lesional Epilepsy
Study Start Date : June 2016
Estimated Primary Completion Date : June 2019
Estimated Study Completion Date : June 2019

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Epilepsy Ultrasound

Arm Intervention/treatment
Experimental: MRgFUS Ablation of Epileptic Foci
MR-Guided Focused Ultrasound
Device: MRgFUS Ablation of Epileptic Foci
MR-Guided Focused Ultrasound
Other Names:
  • MRgFUS
  • FUS
  • Focused Ultrasound
  • MR-Guided Focused Ultrasound




Primary Outcome Measures :
  1. Severity of device and procedure related complications [ Time Frame: At the time of ExAblate Transcranial procedure ]


Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 80 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Men and women, between 18 and 80 years, inclusive.
  2. Patients who are able and willing to give consent and able to attend all study visits.
  3. Seizure refractory to at least three standard antiepileptic medications at adequate doses, failed for lack of efficacy. This may include a rescue medication designated use as PRN.
  4. A minimum of 3 seizures per month for 2 months by patient diary started at intake interview
  5. Subjects should have partial-onset seizures with or without secondary generalization.
  6. Subjects should have evidence suggesting the target lesion is the source of seizures by standard clinical criteria including at least the description of seizures, physical examination, neuroimaging, and video EEG monitoring capturing at least one seizure.
  7. Subjects must be taking 2 medications during the Baseline period and the dosage must be stable.
  8. A diagnosis of intractable epilepsy secondary to a dysplastic subcortical lesion which would include:

    1. Hypothalamic hamartoma
    2. Periventricular nodular hetereotopia
    3. Dysembryoplastic neuroepithelial tumor (DNET)
    4. Cortical dysplasia
    5. Tuberous sclerosis
  9. Subcortical epileptic lesion that is accessible by the ExAblate device.
  10. The targeted lesion is located in the cerebral hemispheres, > 2.5 cm from the inner table of the skull, and within a treatment accessible zone. While multiple epileptic foci may be identified, only one lesion will be targeted.
  11. Lesion(s) are clearly defined on pre-therapy MRI scans.
  12. Size of the tumor is less than 8-cm3 in volume.
  13. Stable doses of all medications during the baseline period based on medical charts of subjects.
  14. Inclusion and exclusion criteria have been agreed upon by two members of the medical team.

Exclusion Criteria:

  1. Patients with unstable cardiac status that would increase anesthetic risk including:

    1. Unstable angina pectoris on medication
    2. Patients with documented myocardial infarction within six months of protocol entry
    3. Congestive heart failure requiring medication (other than diuretic)
    4. Patients on anti-arrhythmic drugs
  2. Patients exhibiting any behavior(s) consistent with ethanol or substance abuse as defined by the criteria outlined in the DSM-IV as manifested by one (or more) of the following occurring within a 12 month period:

    1. Recurrent substance use resulting in a failure to fulfill major role obligations at work, school, or home (such as repeated absences or poor work performance related to substance use; substance-related absences, suspensions, or expulsions from school; or neglect of children or household).
    2. Recurrent substance use in situations in which it is physically hazardous (such as driving an automobile or operating a machine when impaired by substance use)
    3. Recurrent substance-related legal problems (such as arrests for substance related disorderly conduct)
    4. Continued substance use despite having persistent or recurrent social or interpersonal problems caused or exacerbated by the effects of the substance (for example, arguments with spouse about consequences of intoxication and physical fights).
  3. Severe hypertension (diastolic BP > 100 on medication) measured at intake interview or on Treatment Day.
  4. Patients with standard contraindications for MR imaging such as non-MRI compatible implanted metallic devices including cardiac pacemakers, size limitations, etc.
  5. Known intolerance or allergies to the MRI contrast agent (e.g. Gadolinium or Magnevist) including advanced kidney disease
  6. Severely impaired renal function (estimated glomerular filtration rate < 45ml/min/1.73 m2) or receiving dialysis
  7. History of abnormal bleeding and/or coagulopathy
  8. Receiving anticoagulant (e.g. warfarin) or antiplatelet (e.g. aspirin) therapy within one week of focused ultrasound procedure or drugs known to increase risk or hemorrhage (e.g. Avastin) within one month of focused ultrasound procedure; or, unable or unwilling to stop anticoagulant for the purpose of focused ultrasound procedure.
  9. Active or suspected acute or chronic uncontrolled infection
  10. History of intracranial hemorrhage
  11. Cerebrovascular disease (multiple CVA or CVA within 6 months)
  12. Individuals who are not able or willing to tolerate the required prolonged stationary supine position during treatment (can be up to 4 hrs of total table time.)
  13. Symptoms and signs of increased intracranial pressure (e.g. headache, nausea, vomiting, lethargy, and papilledema)
  14. Are participating or have participated in another clinical trial in the last 30 days
  15. Presence of any other neurodegenerative disease
  16. Presence of cognitive impairment severe enough to be unable to understand and consent for the study, or understand the procedures
  17. History of immunocompromise, including patient who is HIV positive
  18. Known life-threatening systemic disease
  19. Patients with current or a prior history of current suicidal ideation or previous suicide attempt within the past year
  20. Patients with risk factors for intraoperative or postoperative bleeding (platelet count less than 100,000 per cubic millimeter, PT > 14, PTT > 36 or INR > 1.3) or a documented coagulopathy
  21. Patients with malignant brain tumors
  22. Any illness that in the investigator's opinion preclude participation in this study.
  23. Pregnancy or lactation.
  24. Legal incapacity or limited legal capacity.
  25. Patients with a known history of psychogenic non-epileptic spells in the last three years.
  26. Patients with a vagal nerve stimulator, deep brain stimulator, other implanted electronic device, or prior radiofrequency lesion techniques.
  27. Patients with cardiopulmonary or vascular illness that would complicate anesthesia.
  28. Patients who are unwilling or unable to undergo general anesthesia.
  29. Lesions in the brainstem or cerebellum.
  30. Treatment of more than one lesion for subjects with multilobar anatomic areas
  31. Subjects with symptomatic generalized epilepsy
  32. Subjects with only simple partial seizures.
  33. Subjects who have had convulsive status epilepticus within 12 months prior to baseline
  34. Subjects with a prior diagnosis of psychogenic/non-epileptic seizures within the last 5 years.
  35. Subjects who are candidates for traditional open surgery or elect to receive traditional open surgery are excluded

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02804230


Locations
United States, Virginia
University of Virginia Recruiting
Charlottesville, Virginia, United States, 22908
Contact: Stacy Thompson    434-982-4315    SRC2H@hscmail.mcc.virginia.edu   
Principal Investigator: Nathan Fountain, MD         
Sponsors and Collaborators
InSightec
Investigators
Principal Investigator: Nathan Fountain, MD University of Virginia

Responsible Party: InSightec
ClinicalTrials.gov Identifier: NCT02804230     History of Changes
Other Study ID Numbers: EP001
First Posted: June 17, 2016    Key Record Dates
Last Update Posted: January 26, 2018
Last Verified: January 2018
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided

Additional relevant MeSH terms:
Epilepsy
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases