Electrophysiology-based Deep Brain Stimulation Programming for Parkinson's Disease
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- Assessment of motor symptoms using the Unified Parkinson's Disease Rating Scale (UPDRS)
研究概览
简要总结
Deep brain stimulation (DBS) effectively alleviates motor symptoms in Parkinson's disease (PD). However, current programming is manual and time-consuming. This study will evaluate physiology-based programming using local field potentials (LFPs) to identify optimal stimulation parameters. Specifically, DBS contact selection based on beta power and a broad-band approach will be compared with conventional clinician-based programming.
详细描述
Up to thirty patients with DBS (unilateral or bilateral leads) attached to a bidirectional implantable pulse generator will be enrolled in this study. This commercially available IPG allows both therapeutic stimulation and chronic sensing. It has been designed to capture local field potentials (LFPs) from implanted DBS leads while delivering stimulation both inside and outside the clinic.
After recording LFP data, then, the physician will perform the traditional clinical monopolar review and determine the optimized DBS settings ('clinician-based' settings) following standard clinical procedures, and without looking at the physiology data. In parallel, the LFP data will be analyzed to identify the 'optimal' therapy contact based on 1) maximum beta power, and 2 ) broad-band multi-frequency analysis.
The physician will then setup up to 4 stimulation programs will be set up:
- Clinician-based programming (standard of care),
- Maximum Beta power-based programming,
- Broad-band programming.
- If needed, second-best clinician-based programming (standard of care)
In this study, settings 1, 2, and 4 (optional) are determined based on established standards of care or manufacturer guidelines. Setting 3, however, is derived using our novel electrophysiology-based algorithm. While the method for determining this setting is innovative, the resulting parameter may be identical to those obtained through conventional approaches (settings 1, 2, or 4). Therefore, although the methodology introduces a new process, the final settings remain within clinically accepted ranges and do not exceed standard clinician-based practices.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Treatment
- 盲法
- Single (Participant)
入排标准
- 年龄范围
- 21 Years 至 89 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients with a diagnosis of idiopathic PD fulfilling the Movement Disorder Society Clinical Diagnostic Criteria for PD
- •DBS implantation with the Percept DBS device (Medtronic, USA) for the treatment of motor symptoms
- •Ability to give informed consent for the study
- •Willingness to do this study at the time of the initial programming session
- •Age 21 to 89 years old
排除标准
- •Inability to comply with the study protocol
- •Atypical Parkinsonism
- •Any personality or mood symptoms that study personnel believe will interfere with the study requirements
研究组 & 干预措施
Clinician-based
干预措施: Clinician-based DBS programming (Device)
Maximum beta power-based
干预措施: Maximum Beta power-based DBS programming (Device)
Broad-band
干预措施: Broad-band electrophysiology-based DBS programming (Device)
结局指标
主要结局
Assessment of motor symptoms using the Unified Parkinson's Disease Rating Scale (UPDRS)
时间窗: From enrollment to end of study (1 month)
The UPDRS (Unified Parkinson's Disease Rating Scale) Motor Scale (Part III) is a clinician-rated tool assessing motor functions like tremor, rigidity, bradykinesia, and gait in Parkinson's disease (PD), using a 0-4 scale for each item, with higher scores indicating greater impairment, helping track disease progression and treatment response.
次要结局
未报告次要终点
