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MR-Guided Functional Ultrasound-Neurosurgery for Movement Disorders

Phase 1
18 Years
80 Years
Not Enrolling
Essential Tremor, Dystonia, Parkinson's Disease

Thank you

Trial Information

MR-Guided Functional Ultrasound-Neurosurgery for Movement Disorders

Inclusion Criteria:

- Men and women, between 18 and 80 years, inclusive.

- Patients who are able and willing to give consent and able to attend all study

- A diagnosis of a MD, such as Essential Tremor, Idiopathic Parkinson's diseases or
primary Dystonia as confirmed from clinical history and examination by a movement
disorder neurologist.

- A MD refractory to adequate medical treatment, or in whom the indication for DBS
would be given, but DBS cannot be performed because of medical comorbidities or
medical reasons, or because the patient clearly confirms by written statement that he
does not want to undergo DBS for personal reasons (PD: increasing motor fluctuations
albeit optimal medical treatment & unbearable side effects of medication; ET: failure
of adequate tremor control with Propranolol and Primidone alone and in combination;
Dystonia: dystonia or pain not controlled by oral medication). An adequate medication
trial is defined as a therapeutic dose of each medication or the development of side
effects as the medication dose is titrated.

- Either the medial thalamic nuclei or the subthalamic or pallidal areas can be target
by the ExAblate device. The target region must be apparent on MRI such that targeting
can be performed with either direct visualization or by measurement from landmarks,
using the "Stereotactic Atlas of the Human Thalamus and Basal Ganglia" by Anne Morel,
39 analogous to our first clinical FUS study on patients with chronic pain 33.

- Able to communicate sensations during the ExAblate MRgFUS treatment

- Stable doses of all medications for 30 days prior to study entry and for the duration
of the study.

- Significant disability due to MD despite medical treatment (speaking, feeding other
than liquids, bringing liquids to mouth, hygiene, dressing, writing, working, and
social activities)

- Inclusion and exclusion criteria have been agreed upon by two members of the medical

Exclusion Criteria:

- Patients with unstable cardiac status including:

- Unstable angina pectoris on medication

- Patients with documented myocardial infarction within six months of protocol

- Congestive heart failure requiring medication (other than diuretic)

- Patients on anti-arrhythmic drugs

- 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:

- 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).

- 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)

- Recurrent substance-related legal problems (such as arrests for substance
related disorderly conduct)

- 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).

- Severe hypertension (diastolic BP > 100 on medication)

- Patients with standard contraindications for MR imaging such as non-MRI compatible
implanted metallic devices including cardiac pacemakers, size limitations, etc.

- Known intolerance or allergies to the MRI contrast agent (e.g. Gadolinium) including
advanced kidney disease

- Severely impaired renal function (estimated glomerular filtration rate < 45ml/min/
1.73 m2) or receiving dialysis

- History of abnormal bleeding and/or coagulopathy

- 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

- Active or suspected acute or chronic uncontrolled infection

- History of intracranial hemorrhage

- Cerebrovascular disease (multiple CVA or CVA within 6 months)

- 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.)

- Symptoms and signs of increased intracranial pressure (e.g. headache, nausea,
vomiting, lethargy, and papilledema)

- Participation in another clinical trial in the last 30 days

- Patients unable to communicate with the investigator and staff.

- Presence of any other neurodegenerative disease like parkinson-plus syndromes
suspected on neurological examination. These include: multisystem atrophy,
progressive supranuclear palsy, dementia with Lewy bodies, and Alzheimer's disease.

- Presence of significant cognitive impairment as determined with a score ≤ 24 on the
Mini Mental Status Examination (MMSE)

- Compromised Immune System, including HIV positive serum status

- Known life-threatening systemic disease

- Patients with a history of seizures within the past year

- Patients with current or a prior history of any psychiatric illness will be excluded.
Any presence or history of psychosis will be excluded. Patients with a significant
mood disorders including depression will be excluded. For the purpose of this study,
we consider a significant mood disorder to include any patient who has:

- been under the care of a psychiatrist for over 3 months

- taken antidepressant medications for greater than 6 months

- has participated in cognitive-behavioral therapy

- been hospitalized for the treatment of a psychiatric illness

- received transcranial magnetic stimulation

- received electroconvulsive therapy

- 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

- Patients with brain tumors

- Any illness that in the investigator's opinion preclude participation in this study.

- Pregnancy or lactation.

- Legal incapacity or limited legal capacity.

Type of Study:


Study Design:

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Basic Science

Outcome Measure:

Lesion Size

Outcome Description:

Size of lesion in the target area for each sonication as a function of applied energy/temperature.

Outcome Time Frame:

3 months

Safety Issue:


Principal Investigator

Ernst - Martin, MD

Investigator Role:

Principal Investigator

Investigator Affiliation:

University Children's Hospital Zurich, Switzerland


Switzerland: Swissmedic

Study ID:

EK: 2012-0027



Start Date:

November 2012

Completion Date:

Related Keywords:

  • Essential Tremor
  • Dystonia
  • Parkinson's Disease
  • FUS
  • focused ultrasound
  • functional brain disorder
  • neuropathic pain
  • movement disorders
  • malignant brain tumors
  • Dystonia
  • Dystonic Disorders
  • Movement Disorders
  • Parkinson Disease
  • Tremor
  • Essential Tremor