跳至主要内容
临床试验/NL-OMON26326
NL-OMON26326尚未招募不适用

Wearable MEG - Using novel technology to improve surgeryoutcome in epilepsy patients

etherlands Epilepsy Foundation (NEF)0 个研究点目标入组 7 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
7

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

入选标准

  • Patients have refractory epilepsy (not responding to treatment with anti-epileptic
  • drugs) and are candidates for epilepsy surgery at VUmc (adults) or UMCU (children).
  • - We include adults (VUmc) or children of six years of age or older (UMCU).
  • - Patients have already undergone a clinical SQUID-based MEG and dEEG at VUmc
  • - 3 patients: confirmed focal source on dEEG of mesial temporal origin
  • - 1 patient: frequent seizures (~daily)
  • - Six years of age or older
  • - Patients have already undergone a clinical SQUID-based MEG with simultaneous
  • scalp-EEG at VUmc
  • - Confirmed focal source of epileptiform activity in clinical MEG or EEG

排除标准

  • - Already undergone surgery for their current epilepsy
  • - The patients have already undergone a clinical SQUID-based MEG. Those patients
  • who had claustrophobic or anxiety experiences from being enclosed in the
  • magnetically shielded room will be excluded
  • - Patients with many artefacts, related to either movement (restlessness, i.e. not
  • seizure-related) or metal implants (not MEG compatible), on their clinical SQUIDbased

研究者

发起方
etherlands Epilepsy Foundation (NEF)

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