Precuneus Mapping With Sinaptistim® (an Investigational TMS-EEG System) in Mild to Moderate AD Patients
Transcranial magnetic stimulation (TMS), electroencephalography (EEG), and combined TMS-EEG approaches have been used in human research to characterize cortical excitability and network-level neurophysiologic responses. The SinaptiStim System is an investigational integrated TMS-EEG platform designed to synchronize TMS delivery, EEG acquisition, and is intended to support standardized characterization of neurophysiologic responses and individualized mapping of stimulation parameters relevant to later therapeutic use.
The rationale for this early single-site, non-treatment study is to obtain initial clinical evidence that the investigational device can be used safely and as intended in participants with mild to moderate Alzheimer's disease (AD), can acquire EEG data of sufficient quality for the planned application, and can be implemented operationally at the clinical site with appropriate training and usability prior to launch of a larger treatment trial.
The study involves two visits, a screening visit with magnetic resonance imaging (MRI) followed by a TMS-EEG mapping visit. Participants who complete this study successfully may be invited to provide informed consent for screening and potential enrollment in a future treatment protocol. This study does not include randomization or a sham control group or therapeutic treatment.
研究概览
研究类型
注册 (估计的)
联系人和位置
学习联系方式
- 姓名:Kara Detlefsen
- 电话号码:720-656-1543
- 邮箱:kara@sinapticatx.com
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
取样方法
研究人群
Patients 65-85 years of age with mild (stage 4) or moderate (stage 5) AD
描述
Inclusion Criteria:
- Must have a reliable study partner with at least 10 hours per week of direct or indirect contact. The study partner must be willing and able to provide informed consent, participate in the study visits and provide information for protocol-required assessments.
- Participant and study partner must each provide signed informed consent before initiation of any study-specific assessments or procedures.
- 65 to 85 years of age
- Stable non-AD medications for at least 4 weeks before signing informed consent
- If treated with a cholinesterase inhibitor for symptoms related to Alzheimer's disease, the dose must be stable for at least 12 weeks before signing informed consent.
- Documented cognitive impairment with decline in memory for more than 6 months before signing informed consent
- Clinical stage 4 or 5 Alzheimer's disease with biological confirmation
- MMSE score 18 to 26 inclusive at Screening
- Screening CDR Global Score of 0.5 to 2.0, with CDR Memory Box score of at least 0.5 plus one additional domain Box score of at least 0.5
Exclusion Criteria:
-
Any contraindication to MRI required by the protocol, including non-compatible implanted metal or electronic devices, ferromagnetic intracranial or other unsafe metallic implants, severe claustrophobia not manageable per site practice, or any other condition making MRI unsafe or not feasible.
-
Current participation in another interventional clinical study, or receipt of any investigational drug, biologic, or device within 3 months before signing informed consent.
-
Prior treatment with an anti-amyloid monoclonal antibody for Alzheimer's disease that is:
- Less than 6 months of continuous treatment immediately before informed consent, or
- Not at a stable label-recommended maintenance dose/maximally tolerated dose, or
- Interrupted for > 8 consecutive weeks during that 6-month period, or
- Associated at any time prior to informed consent with ARIA-E or ARIA-H (including microhemorrhage, superficial siderosis, or macro hemorrhage) that resulted in temporary or permanent interruption, delay, or discontinuation of anti-amyloid monoclonal antibody treatment.
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Current use of, or plan to initiate any brain stimulation therapy before completion of this study.
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Current use of medications that may alter cortical excitability, seizure threshold, sedation, or interpretation of treatment response.
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Clinical history, laboratory findings, or neuroimaging findings consistent with any significant clinical neurodegenerative or neurologic disorder, cerebrovascular disease, structural intracranial abnormality or central nervous system lesion that may increase risk with TMS or confound study assessments.
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History of seizure disorder, epilepsy, unprovoked seizure, or any seizure considered by the investigator to indicate increased risk with TMS.
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Any condition that, in the opinion of the investigator, makes the participant unsuitable for the study, including inability to comply with study requirements.
学习计划
研究是如何设计的?
设计细节
- 观测模型:COHORT
- 时间观点:PROSPECTIVE
队列和干预
团体/队列 |
干预/治疗 |
|---|---|
|
Observational Mild to Moderate AD Cohort
We will enroll up to 30 adults, age 65 to 85, with clinical stage 4 or 5 AD including biological confirmation. Eligible participants will have a MRI and complete a TMS-EEG mapping session. |
A non-therapeutic transcranial magnetic stimulation (TMS) combined with electroencephalography (EEG) assessment to evaluate cortical excitability and network-level brain responses.
其他名称:
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Proportion of participants with quality EEG recordings
大体时间:Enrollment through study completion, approximately 6 weeks per participant and 6 months for entire study cohort
|
Proportion of enrolled participants with successful completion of the protocol-defined device mapping procedure and acquisition of EEG data meeting predefined quality criteria |
Enrollment through study completion, approximately 6 weeks per participant and 6 months for entire study cohort
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Procedural safety and device-related events
大体时间:Enrollment through study completion, approximately 6 weeks per participant and 6 months for entire study cohort
|
Incidence of device-related adverse events, adverse device effects, serious adverse events, and device deficiencies observed during the study visit and immediate post-procedure period. |
Enrollment through study completion, approximately 6 weeks per participant and 6 months for entire study cohort
|
|
Proportion of completed TMS-EEG mapping sessions
大体时间:Enrollment through study completion, approximately 6 weeks per participant and 6 months for entire study cohort
|
Proportion of attempted sessions completed per protocol without major technical failure and with EEG data meeting predefined technical quality criteria. |
Enrollment through study completion, approximately 6 weeks per participant and 6 months for entire study cohort
|
|
Critical-task Success Ratings from Site Staff
大体时间:Study start through study closeout, approximately 6 months
|
Site staff critical-task success and structured ratings of ease of use, workflow fit, and training adequacy. This will be assessed via clinician and technician interviews using sponsor developed questionnaires and interviews. |
Study start through study closeout, approximately 6 months
|
|
Screening, eligibility, and enrollment feasibility
大体时间:Study start through study closeout, approximately 6 months.
|
Number screened, number eligible, number enrolled, proportion eligible, and reasons for screen failure or non-enrollment. |
Study start through study closeout, approximately 6 months.
|
合作者和调查者
调查人员
- 学习椅:Giacomo Koch, MD, PhD、Sinaptica Therapeutics, Inc.
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他研究编号
- ST-902
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
在美国制造并从美国出口的产品
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