Directional Bilateral Thalamic Patterned Stimulation (Chronos)

Официальное название

Directional Bilateral Thalamic Patterned Stimulation in Individuals with Essential Tremor

Обзор

Population Size and Eligible Patients: The investigators aim to recruit 5 to 10 patients with tremors who have previously undergone Ventral Intermedius Deep Brain Stimulation (VIM-DBS) treatment but have experienced early or late loss of benefits. Additionally, the investigators will enroll ten patients with essential tremor who require VIM-DBS surgery. These individuals will undergo bilateral implantation of Boston Scientific Genus Implantable Pulse Generator (IPG) devices, connected to Boston Scientific Cartesia™ 8-contact Directional Leads. Study Design: This study comprises two distinct phases. Phase 1 is a cross-sectional investigation designed to identify the optimal algorithm for patterned stimulation in the VIM region . Phase 2 is a prospective clinical trial focusing on the assessment of safety and efficacy of bilateral VIM-DBS in patients with essential tremor. Objectives: The primary objective in Phase 2 is to evaluate the safety and effectiveness of bilateral VIM-DBS in individuals with essential tremor. In Phase 1, the investigators seek to explore the impact of the Chronos programming software on tremor patients who have experienced early or late loss of benefits.

Вмешательства

• Другое DBS programing
  The physician will utilize the Boston Scientific Chronos Clinician Programmer (software) to make adjustments to the Deep Brain Stimulation (DBS) settings for the patients.

Первичные конечные точки

• Tremor Rating Scale (Part A-B) [Срок оценки: Phase 1-Baseline]
• Tremor analysis [Срок оценки: Phase 1-Baseline]
• Tremor Rating Scale (A-C) [Срок оценки: Phase 2-Baseline, Month 2, Month 4, Month 6, Month 8]
• Tremor analysis (meter per second squared) [Срок оценки: Phase 2-Baseline, Month 2, Month 4, Month 6, Month 8]
• Gait speed (meter per second) [Срок оценки: Phase 2-Baseline, Month 2, Month 4, Month 6, Month 8]
• Base of support (meter) [Срок оценки: Phase 2-Baseline, Month 2, Month 4, Month 6, Month 8]
• Step length (meter) [Срок оценки: Phase 2-Baseline, Month 2, Month 4, Month 6, Month 8]
• Stride length (meter) [Срок оценки: Phase 2-Baseline, Month 2, Month 4, Month 6, Month 8]
• Single stance time and double stance time (seconds) [Срок оценки: Phase 2-Baseline, Month 2, Month 4, Month 6, Month 8]
• Tandem gait [Срок оценки: Phase 2-Baseline, Month 2, Month 4, Month 6, Month 8]

Критерии участия

Критерии включения

• Phase 1: 5 to 10 tremor patients already treated with VIM-DBS but not doing well due to early and/or late loss of benefits (i.e. tremor scores ON stimulation identical or greater than before surgery in absence of stimulation).
• Phase 2: 10 Essential Tremor patients in need of DBS surgery.
• Written and signed Informed Consent.
• Age 18 to 85 years old.
• Subject must have Essential Tremor, as defined by all the following criteria: (a) isolated tremor syndrome consisting of bilateral action tremor; (b) at least three years duration; and (c) with or without tremor in other locations (e.g., head, voice, or low limbs) \[1\].
• Soft signs (categorizing patients as Essential Tremor-plus) will be allowed and noted in the patient's chart.
• Subject must be on stable dose of anti-tremor medication for at least 4 weeks prior to screening.
• Subject had no botulinum injection for at least three months prior to screening.
• Subject does not have a significant other medical condition biasing the study finding in investigator's opinion.

Критерии исключения

• Unwilling or inability to follow the procedures specified by the protocol.
• Presence of significant psychiatric or cognitive condition likely to compromise the subject's ability to comply with requirements of the study protocol.
• Untreated clinically significant depression.
• Any current drug or alcohol abuse, as determined by the investigator.
• History of suicidal attempt within the last 1 year prior to consent or current active suicidal ideation as determined by the investigator.
• Any significant medical condition that is likely to interfere with study procedures or likely to confound evaluation of study endpoints.
• Any terminal illness with life expectancy of < 12 months.
• Participation in any other interventional clinical trial (e.g. drug, device).

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение

Нерандомизированное

Модель

Параллельные группы

Маскирование

Открытое

Основная цель

Лечение

Центры проведения

Канада · 1 центр

• Movement Disorders Centre - Toronto Western Hospital — Toronto

Идентификаторы

NCT: NCT06325852 · 22-5772

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

Открыть это исследование на ClinicalTrials.gov ↗