| Eligibility |
Inclusion Criteria:
1. Subjects who:
1. previously underwent Exablate thalamotomy for their essential tremor in a
clinical study or in a commercial procedure at least 9 months prior to enrolling
in this study for contralateral Exablate thalamotomy
2. Subjects who would benefit from a bilateral treatment for their essential tremor
and would want to undergo a staged bilateral thalamotomy
2. All subjects must have a complete baseline CRST prior from first Exablate thalamotomy
3. Men and women age 22 years to 75 years of age.
4. Minimum score of 24 on MoCA or 20 on MMSE
5. Subjects who are able and willing to give consent and able to attend all study visits
6. Postural or intention tremor severity score of greater than or equal to 2 in the both
upper extremities as measured by the CRST rating scale while on stable medication
7. Thalamus can be targeted by the Exablate device. The region must be apparent on MRI
such that targeting can be performed.
8. Able to communicate sensations during the Exablate Thalamotomy treatment
9. Original (before first Exablate procedure) CRST score of 2 or above in any one of the
items 16-23 from the Disability subsection of the CRST: speaking, feeding other than
liquids, bringing liquids to mouth, hygiene, dressing, writing, working, and social
activities.
10. Subjects on antidepressant medications must be stable for at least 3 months prior to
procedure(i.e., no change in medication drug or dosage for 3 months based on
historical medical records).
11. Remains eligible for Exablate treatment with no changes to medical history that would
affect Exablate treatment criteria, (e.g., bleeding/coagulation requirements, or new
pathology such as infarct, tumor, etc).
Exclusion Criteria:
1. Subjects with unstable cardiac status
2. Subjects 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:
3. Subjects with uncontrollable blood pressure (hypertensive with diastolic BP > 100 on
medication)
4. History of abnormal bleeding and/or coagulopathy, i.e. subjects with risk factors for
intraoperative or postoperative bleeding as indicated by: platelet count less than
100,000 per cubic millimeter, a documented clinical coagulopathy, or INR coagulation
studies exceeding the institution's laboratory standard
5. 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
6. Active or suspected acute or chronic uncontrolled infection
7. 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.)
8. Subjects with life-threatening systemic disease that include but not limited to the
following will be excluded from the study participation: HIV, Liver Failure, blood
dyscrasias, etc...
9. Any clinically significant moderate to severe sensory deficit lasting greater than 30
days after the first Exablate thalamotomy NOTE: Subjects with clinically significant
moderate to severe sensory deficit following first Exablate thalamatomy should be
excluded even if event resolves within a few months of treatment. This may cause new
first thalamotomy subjects to be ineligible for the bilaterally staged treatment.
10. Moderate to severe cerebellar disturbance (imbalance or ataxia) or presence of
moderate or severe hemiparesis NOTE: Subjects with moderate to severe cerebellar
disturbance (imbalance or ataxia) or presence of moderate or severe hemiparesis
following first Exablate thalamatomy should be excluded even if event resolves within
a few months of treatment. This may cause new first thalamotomy subjects to be
ineligible for the bilaterally staged treatment.
11. Any persistent dysphasia/dysarthria, language impairment following first Exablate
thalamotomy.
NOTE: Subjects with significant impairment following first Exablate thalamotomy should
be excluded even if event resolves within a few months of treatment. This may cause
new first thalamotomy subjects to be ineligible for the bilaterally staged treatment.
12. Significant reduction in cognitive function since the first thalamotomy. NOTE:
Subjects with significant reduction in cognitive function following first Exablate
thalamatomy should also be excluded even if event resolves within a few months of
treatment. This may cause new first thalamotomy subjects to be not eligible for the
bilaterally staged treatment.
13. Subject is pregnant or breastfeeding.
14. Subjects who have an overall Skull Density Ratio of less than 0.40 as calculated at
screening
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