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Clinical Trials in Japan / NCT07066358
Recruiting Not applicable

Simultaneous Bilateral Radiofrequency Thalamotomy for Medication-Refractory Essential Tremor

NCT07066358 · tracked via the Priya Life Science Japan tracker
Phase
Not applicable
Started
2025-07-03
Last updated
2025-07-18

Condition(s) studied

Essential Tremor

Investigational drug(s) / intervention(s)

Simultaneous Bilateral RF Thalamotomy

Simultaneous Bilateral RF Thalamotomy: This intervention involves simultaneous bilateral radiofrequency (RF) lesioning of the ventral intermediate nucleus (Vim) of the thalamus using a stereotactic frame under local anesthesia. The procedure begins with RF ablation on the side contralateral to the dominant hand. Intraoperative MRI is then performed to confirm the absence of hemorrhagic complications. If no bleeding or other adverse events are detected, the procedure proceeds to the contralateral Vim. If hemorrhage is identified, the surgery is terminated after unilateral treatment. This technique allows for immediate bilateral tremor reduction in patients with medication-refractory essential tremor, while prioritizing patient safety through intraoperative imaging-based decision-making.

Study summary

This study aims to evaluate the safety and effectiveness of simultaneous bilateral radiofrequency thalamotomy for patients with medication-refractory essential tremor (ET). Essential tremor is a common neurological condition that causes involuntary shaking, often affecting the hands and interfering with daily activities such as writing, eating, or using tools. While medications such as propranolol and primidone can help some patients, others experience limited or no benefit.

In this study, five adult participants diagnosed with essential tremor that does not respond to standard medications will undergo simultaneous bilateral stereotactic radiofrequency lesioning of the ventral intermediate nucleus (Vim) of the thalamus. This procedure involves precisely targeting both sides of the Vim to reduce tremor in both arms during a single surgical session.

Prior to surgery, participants will undergo brain MRI for surgical planning, as well as clinical evaluations including the Clinical Rating Scale for Tremor (CRST), Quality of Life in Essential Tremor Questionnaire (QUEST), the Scale for the Assessment and Rating of Ataxia (SARA), mood scales (BDI, BAI, AES), and cognitive function testing.

The surgery will be performed under local anesthesia using a stereotactic frame and intraoperative imaging. Tremor reduction will be assessed postoperatively and at 1, 3, and 6 months. The primary outcome is the improvement in CRST scores at 6 months. Secondary outcomes include quality of life (QUEST), ataxia symptoms (SARA), mood and cognitive changes, and adverse events.

This research is being conducted at Tokyo Women's Medical University. The study is IRB-approved and participants will be monitored closely throughout the 6-month follow-up period. Any complications or adverse events, such as temporary speech or swallowing difficulties, will be recorded and managed appropriately. The goal of this study is to explore whether performing thalamotomy on both sides simultaneously is a safe and effective treatment option for patients with severe and medication-resistant essential tremor.

Eligibility

Sex
ALL
Min age
20 Years
Max age
70 Years
Healthy volunteers
No
Inclusion Criteria: * Adults aged 20 to 70 years. * Diagnosis of essential tremor by a neurologist or neurosurgeon specializing in movement disorders. * Refractory to standard pharmacological therapy (e.g., propranolol, primidone, benzodiazepines, or alprenolol). * Mini-Mental State Examination (MMSE) score ≥ 27. * Able to undergo MRI. * Provided written informed consent for participation in the study. Exclusion Criteria: * History or evidence of bleeding tendency. * MRI contraindications (e.g., metallic implants, severe claustrophobia). * Presence of intracranial pathology on preoperative MRI that would interfere with surgery. * Pregnant or breastfeeding individuals. * Any other condition that the principal investigator deems inappropriate for study participation.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Tokyo Women's Medical University, Department of Neurosurgery Shinjuku-Ku Tokyo Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07066358 on ClinicalTrials.gov ↗ ← All trials in Japan