High-density Flexible μECoG for Epilepsy Surgery - A Single-Arm ECT (Epi-PRECISE)
2026年8月12日 更新者：Kai Zhang、Beijing Tiantan Hospital
Precision Resection of the Epileptogenic Zone Using Intraoperative Submillimeter Micro-Electrocorticography (Epi-PRECISE): A Single-Arm Trial With an External Historical Control Cohort
What's the clinical value of high-density flexible microelectrocorticography (μECoG) for guiding the resection of epileptogenic zone (EZ) in epilepsy surgery?
研究概览
地位
招聘中
详细说明
- Compare the effect of intraoperative high-density flexible μECoG guidance versus no intraoperative μECoG guidance on surgical prognosis in patients with drug-resistant focal epilepsy.
- Explore intraoperative electrophysiological biomarkers recorded by high-density μECoG that are associated with surgical prognosis.
研究类型
介入性
注册 (估计的)
85
阶段
- 不适用
联系人和位置
本节提供了进行研究的人员的详细联系信息，以及有关进行该研究的地点的信息。
学习联系方式
- 姓名：Kai Zhang Dr
- 电话号码：86 01059975051
- 邮箱：zhangkai62035@sina.com
学习地点
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Beijing Municipality
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Beijing、Beijing Municipality、中国、100070
- 招聘中
- Beijing Tiantan Hospital
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接触：
- Du Cai Dr
- 电话号码：86 01059975051
- 邮箱：ferryc22@163.com
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-
参与标准
研究人员寻找符合特定描述的人，称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
- 孩子
- 成人
接受健康志愿者
不
描述
Inclusion Criteria:
- Age 3 to 60 years.
- Diagnosis of drug-resistant epilepsy, defined as persistent seizures despite treatment with two or more appropriately selected, adequately dosed and adequately tried antiseizure medications.
- Diagnosis of focal epilepsy after standard presurgical evaluation and considered suitable for resective epilepsy surgery.
- Preoperative cognitive or developmental status sufficient to participate in study assessments, as judged by the investigator and assessed using age-appropriate validated instruments. For participants aged 3 to 6 years, developmental status must be within the normal range according to the Griffiths Mental Development Scales. For participants aged 6 to 16 years, cognitive function must be within the normal range according to the Wechsler Intelligence Scale for Children. For participants older than 16 years, a Mini-Mental State Examination score of 24 or higher will be required.
- Written informed consent provided by the participant or, when applicable, by a legal guardian.
Exclusion Criteria:
- Suspected mesial temporal lobe epilepsy after multidisciplinary presurgical evaluation.
- History of any previous neurosurgical craniotomy before epilepsy surgery.
- Severe psychiatric, cognitive, or psychological disorder that prevents participation in the study or completion of follow-up.
- Contraindication to surgery.
学习计划
本节提供研究计划的详细信息，包括研究的设计方式和研究的衡量标准。
研究是如何设计的？
设计细节
- 主要用途：治疗
- 分配：不适用
- 介入模型：单组作业
- 屏蔽：无（打开标签）
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的：Intraoperative application of high-density flexible μECoG-Guided Resection
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During resective epilepsy surgery, a sterile high-density flexible microelectrocorticography will be placed on the exposed cortical surface over the suspected epileptogenic zone and adjacent cortex.
The array will be used for high-spatial-resolution intraoperative μECoG recording and real-time analysis of epileptiform activity, including interictal spikes, high-frequency oscillations, spatial discharge gradients, and propagation patterns.
The intraoperative ECoG findings will be provided to the surgical team to assist in defining the epileptogenic zone and tailoring the extent of resection.
The high-density μECoG is used for intraoperative recording only and will be removed before wound closure.
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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 |
|---|---|---|
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Seizure Freedom Rate at 6 Months After Surgery
大体时间：From surgery to 6 months postoperatively
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The proportion of participants who remain free from any type of epileptic seizure during the 6-month postoperative follow-up period.
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From surgery to 6 months postoperatively
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Seizure Freedom Rate at 1 Year After Surgery
大体时间：From surgery to 1 year postoperatively
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The proportion of participants who remain free from any type of epileptic seizure during the 1-year postoperative follow-up period.
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From surgery to 1 year postoperatively
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Postoperative Seizure Outcome According to ILAE Classification
大体时间：6 months and 1 year postoperatively
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Postoperative seizure outcome will be evaluated using the International League Against Epilepsy classification at 6 months and 1 year after surgery.
ILAE class 1 indicates complete seizure freedom without aura, and higher classes indicate worse seizure outcomes.
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6 months and 1 year postoperatively
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Monthly Seizure Frequency
大体时间：Baseline, 6 months postoperatively, and 1 year postoperatively
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Monthly seizure frequency will be assessed before surgery and at 6 months and 1 year after surgery.
The measure is defined as the average number of epileptic seizures per month.
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Baseline, 6 months postoperatively, and 1 year postoperatively
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Postoperative Complications
大体时间：Perioperative period, 6 months postoperatively, and 1 year postoperatively
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The incidence of postoperative complications, including infection, fever, neurological deficits, and other surgery-related complications, will be recorded during the perioperative period and postoperative follow-up.
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Perioperative period, 6 months postoperatively, and 1 year postoperatively
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Surgery-Related Adverse Events
大体时间：Perioperative period
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The incidence of surgery-related adverse events will be recorded during the perioperative period.
Adverse events include events directly related to the surgical procedure.
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Perioperative period
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Serious Adverse Events
大体时间：Perioperative period
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The incidence of serious adverse events, including postoperative death or severe deterioration of health status during the perioperative period, will be recorded.
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Perioperative period
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Seizure Severity Assessed by the National Hospital Seizure Severity Scale
大体时间：Baseline, 6 months postoperatively, and 1 year postoperatively
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Seizure severity will be assessed using the National Hospital Seizure Severity Scale (NHS3) before surgery and at 6 months and 1 year after surgery.
The NHS3 is a seizure severity scale with scores ranging from 1 to 27, with higher scores indicating more severe seizures and therefore a worse outcome.
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Baseline, 6 months postoperatively, and 1 year postoperatively
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Developmental Function Assessed by the Griffiths Mental Development Scales
大体时间：Baseline, 6 months postoperatively, and 1 year postoperatively
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For participants aged 3 to 6 years, developmental function will be evaluated using the Griffiths Mental Development Scales before surgery and at 6 months and 1 year after surgery.
The primary reported score will be the General Developmental Quotient or General Quotient.
The quotient score ranges from 50 to 150, with higher scores indicating better developmental function and therefore a better outcome.
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Baseline, 6 months postoperatively, and 1 year postoperatively
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Cognitive Function Assessed by the Wechsler Intelligence Scale for Children
大体时间：Baseline, 6 months postoperatively, and 1 year postoperatively
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For participants aged 6 to 16 years, cognitive function will be evaluated using the Wechsler Intelligence Scale for Children before surgery and at 6 months and 1 year after surgery.
The primary reported score will be the Full Scale Intelligence Quotient.
The Full Scale Intelligence Quotient standard score ranges from 40 to 160, with higher scores indicating better cognitive function and therefore a better outcome.
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Baseline, 6 months postoperatively, and 1 year postoperatively
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Cognitive Function Assessed by the Mini-Mental State Examination
大体时间：Baseline, 6 months postoperatively, and 1 year postoperatively
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For participants older than 16 years, cognitive function will be evaluated using the Mini-Mental State Examination (MMSE) before surgery and at 6 months and 1 year after surgery.
The MMSE total score ranges from 0 to 30, with higher scores indicating better cognitive function and therefore a better outcome.
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Baseline, 6 months postoperatively, and 1 year postoperatively
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Quality of Life Assessed by the Quality of Life in Epilepsy Inventory-31 or the Pediatric Quality of Life Inventory Version 4.0
大体时间：Baseline, 6 months postoperatively, and 1 year postoperatively
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Quality of life will be evaluated before surgery and at 6 months and 1 year after surgery.
Adult participants will be assessed using the Quality of Life in Epilepsy Inventory-31 (QOLIE-31), and pediatric participants will be assessed using the Pediatric Quality of Life Inventory Version 4.0 (PedsQL 4.0).
Both scales are transformed to scores ranging from 0 to 100, with higher scores indicating better quality of life and therefore a better outcome.
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Baseline, 6 months postoperatively, and 1 year postoperatively
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合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
出版物和有用的链接
负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。
一般刊物
- Guo J, Wang Z, van 't Klooster MA, Van Der Salm SM, Leijten FS, Braun KP, Zijlmans M. Seizure Outcome After Intraoperative Electrocorticography-Tailored Epilepsy Surgery: A Systematic Review and Meta-Analysis. Neurology. 2024 Jun 11;102(11):e209430. doi: 10.1212/WNL.0000000000209430. Epub 2024 May 20.
- Xingjian Liu, Chao Zhang, Baotian Zhao, et al., Preliminary application study of flexible high-density cortical electrodes in assisting localization of epileptogenic zones during epileptogenic zonectomy, Chinese Journal of Neurosurgery, 2025, 41(12):1237-1244. DOI:10.3760/cma.j.cn112050-20250919-00362
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查，以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (估计的)
2026年9月1日
初级完成 (估计的)
2028年7月31日
研究完成 (估计的)
2028年12月31日
研究注册日期
首次提交
2026年6月15日
首先提交符合 QC 标准的
2026年6月15日
首次发布 (实际的)
2026年6月18日
研究记录更新
最后更新发布 (实际的)
2026年8月13日
上次提交的符合 QC 标准的更新
2026年8月12日
最后验证
2026年6月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索，没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求，请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改，我们的网站上也会自动更新.