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临床试验/NCT06105645
NCT06105645招募中不适用

Contribution of Fast-ripples to the Improvement of the Neurosurgical Management of Drug-refractory Epilepsy

University Hospital, Toulouse16 个研究点 分布在 1 个国家目标入组 440 人开始时间: 2024年1月19日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
440
试验地点
16
主要终点
Contribution of fast-ripples information on freedom seizures

研究概览

简要总结

The main aim of this study is to evaluate the contribution of fast-ripples (FR) information on the neurosurgery management of patients with drug-refractory epilepsy investigated by Stereo-ElectroEncephaloGraphy (SEEG), as measured by freedom from disabling seizures one-year post-surgery.

220 patients (for whom 4-6 usual clinical macro-electrodes will be replaced by hybrid micro-macro electrodes and for whom fast-ripples will be assessed) distributed over 5 centres and 220 control patients(who will undergo an SEEG with the usual electrodes and for whom fast-ripples will not be assessed) distributed over 6 centres. This is a controlled, non-randomized, parallel plan, prospective, multicentre exploratory study.

详细描述

This is a controlled, non-randomized, parallel plan, prospective, multicentre exploratory study. The design of the study relies on two groups of patients benefiting from a SEEG, equivalent in size: one with standard and hybrid electrodes for which fast-ripple information will be available for the neurosurgery decision, the other, who will serve as a control group, with standard electrodes only and for which no information regarding fast-ripples will be provided. For all patients undergoing SEEG, the decisions about eligibility to epilepsy surgery and, if eligible, about the best surgical plan, are taken during a multidisciplinary epilepsy meeting (MEM) within the 4 +/- 2 months following the SEEG. In the group of patients with standard and hybrid electrodes, the procedure as extensively tested previously, is to plan the implantation of the standard electrodes as usually done, and once done, to replace from 4 to 6 standard electrodes with hybrid electrodes. In this group, intracerebral ElectroEncephaloGraphy (EEG) data will be acquired for detection of fast-ripples, during one hour of a rest period for 2 days during the first week of SEEG, as well as during one cycle of night sleep when possible. Fast-ripples(number, localization and characteristics) for all these patients will be analysed by an expert group of neuroscientists based in Toulouse blind to the analysis of the Epileptogenic Zone (EZ), irritative and propagation zones and on all micro- and macro contacts, to the participating centre and to the period of recording. The results of the fast-ripple assessment will be provided to the clinicians on time for the MEM. They will incorporate this information along other usual clinical information gathered during the SEEG to reach a conclusion regarding the possibility of a neurosurgery. No analysis of the fast-ripples will be performed in the other group of patients with standard electrodes only. In this group, the conclusion regarding the possibility of a neurosurgery will thus be done during the MEM with the standard clinical information gathered during the SEEG only. Following epilepsy surgery, the typical follow-up performed in routine in all participating centres includes a clinical evaluation one year after surgery, during which Engel class is assessed.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patient suffering from drug-resistant focal epilepsy (DRFE), as defined by the International League Against Epilepsy, undergoing SEEG, the indication of which was selected during a multidisciplinary epilepsy meeting
  • Patient who has given written informed consent to allow the study data collection procedures
  • Patient covered by the French healthcare system.

排除标准

  • Patients under juridical protection (authorship, curators or safeguarding of justice).
  • Patient deprived of liberty by a judicial or administrative decision
  • Patient with a cardiac defibrillator
  • Thermocoagulation planned on one of the potential hybrid electrodes .
  • Patient in exclusion period of another study.
  • No other non-inclusion criteria since the study will only be proposed to patients who already meet the criteria for a SEEG

结局指标

主要结局

Contribution of fast-ripples information on freedom seizures

时间窗: 12 months after epilepsy surgery

Proportion of patients with Engel class I after one-year post-surgery in the group of patients with information of fast-ripples compared to patients without.

次要结局

  • Evolution of quality of life using the score of Quality of life Epilepsy Inventory Epilepsy Inventory(12 months after epilepsy surgery)
  • Distribution of the fast-ripples(Day 0 (SEEG visit))
  • Number of fast-ripples recorded according to the period(Day 0 (SEEG visit))
  • Contribution of fast-ripples information on improvement of epilepsy(12 months after epilepsy surgery)
  • Contribution of fast-ripples information on patients addressed to neurosurgery(12 months after epilepsy surgery)
  • Adverse effects related to Stereo-electroencephalography(Day 0 (SEEG visit))
  • Post-operative neurological deficit(12 months after epilepsy surgery)
  • Level of satisfaction(12 months after epilepsy surgery)
  • Adverse effects of epilepsy surgery(6 months after surgical decision)
  • Recording of fast-ripples(Day 0 (SEEG visit))
  • Adverse effects of hybrid electrodes(Day 0 (SEEG visit))

研究者

申办方类型
Other
责任方
Sponsor

研究点 (16)

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