International, Multicenter, Investigator Blinded, Randomized And Controlled Essential Tremor Trial With Staged-Bilateral FUS
Trial Snapshot
- Phase
- Not Applicable
- Status
- Recruiting
- Sponsor
- InSightec
- Enrollment
- 100
- Locations
- 13
- Primary Endpoint
- Treated Upper Limb Clinical Rating Scale for Tremor (CRST) (A+B) (0-28) score for the treated side.
Study Overview
Brief Summary
This is a post-market (Phase IV) randomized, controlled, blinded, multicenter study with the aim to determine the added value of staged bilateral Exablate thalamotomy compared to a group of patients on previous unilateral treatment combined with local standard medical treatment.
Detailed Description
In patients who have undergone previous unilateral Exablate thalamotomy for Essential Tremor, the aim of this trial is to determine the effect of staged bilateral Exablate thalamotomy compared to a group of patients on previous unilateral treatment. The effect will be measured on tremor reduction, functional impairment, disease-specific quality of life, adverse events and patient-perception of the overall treatment result in patients eligible for a staged bilateral Exablate procedure.
Patients assigned to the treatment arm will receive staged bilateral Exablate thalamotomy. Patients assigned to control group will remain under local standard medical treatment.
The primary efficacy study objective is to demonstrate that Exablate staged-bilateral thalamotomy treatment reduces tremor, as measured by Treated Upper Limb CRST (A+B) (0-28) score, to a higher extent than those remaining on previous unilateral Exablate thalamotomy at 6 months.
The primary safety study objective is to assess the adverse events (AEs) of Exablate staged-bilateral thalamotomy treatment in comparison to those remaining on unilateral treatment (control group) plus medical treatment, including AE type, incidence, severity and duration at 6 months.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- Single (Outcomes Assessor)
Masking Description
Subjects will be videotaped while undergoing a standardized total CRST assessment at baseline and at the 6-month visit (use a standardized video-protocol). Subjects will wear head covers so that the investigator cannot tell whether the patient has received hair shaving to prepare for the FUS-intervention. Video-recordings will be assessed by two blinded core reviewers (i.e., certified Movement Disorder Neurologists, selected by the study Steering Committee (SC) for this task).
The video recordings are played in random order with respect to patients and study time points to minimize reviewer bias.
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Men and women with an age of 18 years or older (according to local labeling).
- •Willing to participate in the study (i.e., signed ICF). (Willing to be randomized).
- •Patient is able to undergo a high-resolution Computerized Tomography (CT) scan.
- •Patient is able to fit into MRI unit and comply with all contraindications for the specific magnetic resonance (MR) system including and limited to contrast medium should there be needed.
- •The thalamus, sub-thalamus and the pallidum must be apparent on MR imaging.
- •Patient is able to communicate sensations to the physician during the procedure; Procedure does not require general anesthesia.
- •Patient must be able to use the Stop Sonication button freely.
- •Patient willing to have their head shaved prior to the actual treatment.
- •Patient has no history for claustrophobia which is not responding to medications.
- •ET patients who are eligible for second side staged bilateral Exablate thalamotomy treatment (according to local labeling). Time since first intervention is at least 9 months.
- •Available tremor assessment prior to the unilateral Exablate thalamotomy.
- •Patients randomized to the study, irrespective of group allocation should be willing and able to remain in the study for at least 6 months and able to complete the required assessments.
Exclusion Criteria
- •Subject experienced any non-transient neurological event or worsening following the previous Exablate procedure.
- •Patients with MRI related contraindications (e.g. presence of metallic implants incompatibility with MRI, severe claustrophobia, reaction to contrast medium).
- •Patients in whom it is not possible to avoid energy absorbing structures or sensitive tissues (e.g., skull implants, surgical clips, shunts, electrodes, dura patch, skull patch, electrodes, etc.) from the path of the ultrasound beam.
- •Patients with concurrent active infections disease and/or severe allergies with fever.
- •Patients that have been diagnosed with brain tumors or a vascular anomaly.
- •Patients with a history of seizures, brain hemorrhages, stroke within the past year, or any coagulopathy.
- •Patients under anticoagulants and/or anti-platelets drugs known to increase bleeding risk within the duration defined by the half-life of the specific drugs.
- •Patient that has been given any contrast agent (e.g., CT, MRI), within 24 hours before treatment
- •Severe unstable hypertension that cannot be controlled by medications (diastolic Blood Pressure > 100 on medication).
- •Patients with unstable cardiac status.
- •Patients exhibiting any behavior(s) consistent with ethanol or substance abuse.
- •Cerebrovascular disease (multiple CVA or CVA within 6 months).
- •Patients with risk factors for intraoperative or postoperative bleeding.
- •Imaging shows abnormal finding in CT or/and MRI (e.g., brain tumor, brain vascular malformation, shunt, etc.).
- •Patient has physical subscale score ≥ 16.5 on the Dysphagia Handicap Index or has been diagnosed with dysphagia.
- •Patient with cognitive impairment.
- •Patient with clinically significant abnormal speech function as determined by a speech pathologist.
Arms & Interventions
Control Arm
Subjects will continue with their standard of care treatment for 6 months.
Intervention: Local standard medical treatment after previous Exablate unilateral thalamotomy. (Other)
Exablate Arm
Subjects will receive staged bilateral Exablate thalamotomy.
Intervention: Staged bilateral Exablate thalamotomy (Procedure)
Outcomes
Primary Outcomes
Treated Upper Limb Clinical Rating Scale for Tremor (CRST) (A+B) (0-28) score for the treated side.
Time Frame: 6 Months
The primary endpoint is the difference of the Treated Upper Limb CRST (A+B) score between groups at 6 months. Higher score means a worse tremor.
Secondary Outcomes
- Treated Upper Limb Clinical Rating Scale for Tremor (CRST) (A+B) (0-28) score as assessed by the blinded reviewers of the video-recordings.(6 Months, 12 Months)
- Clinical Rating Scale for Tremor (CRST) part A (0-76)(6 Months, 12 Months)
- Quality of life questionnaire(6 Months, 12 Months)
- Bilateral Upper Limb Clinical Rating Scale for Tremor (CRST) (A+B) (0-56)(6 Months, 12 Months)
- Total Clinical Rating Scale for Tremor (CRST) (A+B) (0-116)(6 Months, 12 Months)
- Clinical Rating Scale for Tremor (CRST) part C (0-32)(6 Months, 12 Months)
- Axial Clinical Rating Scale for Tremor (CRST) (0-20)(6 Months, 12 Months)
- Change of tremor medication(6 Months, 12 Months)
- Safety: Incidence and frequency of adverse events related to the treatment.(6 Months, 12 Months)