A Study to Evaluate the Safety and Efficacy of Staged Bilateral Magnetic Resonance-Guided Focused Ultrasound Thalamotomy for the Treatment of Essential Tremor (ET-Bi-MRgFUS)

Chinese PLA General Hospital (301 Hospital)

Status: Invitation-only

Conditions: Essential Tremor; Essential Tremor, Movement Disorders

Treatments: Procedure: ExAblate

Study type: Interventional

Funder types: Other

Identifiers

NCT06676501

301ET-2

Details and patient eligibility

About

The objective of this prospective, single-arm, open-label study is to asses the safety and efficacy of the staged bilateral thalamotomy using transcranial magnetic resonance guided focused ultrasound system ExAblate 4000, InSightec Ltd.

Enrollment: 20 estimated patients

Sex: All

Ages: 22+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Men and women age 22 years or older
2. Subject is able and willing to give consent and able to attend all study visits
3. Subject is diagnosed with Essential Tremor as confirmed by a movement disorder specialist
4. Subject's tremor is refractory to adequate trials of at least two medications, one of which being a first line therapy of either propranolol or primidone. 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.
5. Subject is diagnosed with medication-refractory Essential Tremor
6. A subject who underwent an Exablate index procedure in a clinical trial or in a commercial setting at least 9 months prior to enrolling in this trial
7. Subject has a baseline CRST Part A score of 2 or above for postural or intention tremor severity in the upper extremity for the contralateral tremor side while on stable medication
8. Subject is able to communicate sensations during the Exablate thalamotomy procedure.
9. Subject has a baseline CRST Part C score of 2 or above in any one of the items (speaking, eating, drinking, hygiene, dressing, writing, working, and social activities).

Exclusion criteria

1. Subject experienced any non-transient neurological event or worsening following the Exablate index procedure

2. Subject has physical subscale score ≥ 16.5 on the Dysphagia Handicap Index or has been diagnosed with dysphagia

3. Subject has score <22 on the Montreal Cognitive Assessment (MoCA)

4. Subject has any non-transient hemiparesis as determined by physical examination

5. Subject with clinically significant abnormal speech function as determined by a speech pathologist

6. Subject of childbearing potential is pregnant or breastfeeding

7. Subject with unstable cardiac status including:

   1. Unstable angina pectoris on medication
   2. documented myocardial infarction within six months of enrollment
   3. Unstable or worsening congestive heart failure
   4. History of a hemodynamically unstable cardiac arrhythmia
   5. Cardiac pacemaker
   6. Severe hypertension (diastolic BP > 100 on medication)

8. Subjects exhibiting any behavior(s) consistent with ethanol or substance abuse

9. Subject has history of abnormal systemic or intracranial bleeding, hemorrhage, or coagulopathy

10. Subject has abnormal coagulation profile: (PLT < 100,000/μl), PT (>14 sec) or PTT (>36 sec), and INR > 1.3

11. Subject receiving anticoagulant (e.g. warfarin) or antiplatelet (e.g. aspirin) therapy within one week of Exablate procedure or drugs known to increase risk or hemorrhage (e.g. Avastin) within one month of Exablate procedure

12. Subject with cerebrovascular disease, including but not limited to, intracranial aneurysms, dural arteriovenous malformations (AVM), stroke, intracranial atherosclerotic disease, dural arteriovenous fistulas (AVF)

13. Subject with an intracranial tumor

14. Subject with active or suspected acute or chronic uncontrolled infection

15. Subject had deep brain stimulation or a prior stereotactic ablation of the basal ganglia or thalamus

16. Patients with implanted objects in the skull or the brain

17. More than 30% of the skull area traversed by the sonication pathway is covered by scars, scalp disorders (e.g., eczema), or atrophy of the scalp

18. Subjects who have been administered botulinum toxins into the arm, neck, or face for 5 months prior to Baseline.

19. Subject has an overall Skull Density Ratio of less than 0.40 (±0.05) as calculated at screening

20. Subject is unable or willing to tolerate the required prolonged stationary supine position during Exablate procedure (approximately 2-3 hours)

21. Subject is currently participating in another clinical investigation with an active treatment arm

22. Subject is unable to communicate with the investigator and staff

23. Subject is considered to be a poor surgical or study candidate, which may include, but is not limited to the following: any medical, social, or psychological problem that could complicate the required procedures and evaluations of the study in the judgment of the investigator

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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20 participants in 1 patient group

ExAblate Treatment

Experimental group

Description:

Participants will undergo a thalamotomy contralateral to their previous treatment with MRgFUS

Treatment:

Procedure: ExAblate