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Study identifier: NCT07064421 Synced from ClinicalTrials.gov · July 29, 2026
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Non-Helium Magnetoencephalography in Pediatric Refractory Epilepsy

Condition: Refractory Epilepsy in Children  ·  Sponsor: Guangzhou Women and Children's Medical Center

PhaseN/A
Planned participants100
Who can joinAll sexes, 3 Years to 18 Years
Healthy volunteersNo

About this study

The goal of this observational study is to evaluate the effectiveness of Magnetoencephalography (MEG) in the preoperative assessment of children with refractory epilepsy, particularly in identifying the seizure focus, and to compare it with the gold standard methods of Stereo-electroencephalography (SEEG) and Electrocorticography (ECoG). The main questions this study aims to answer are: 1. How consistent is MEG with SEEG/ECoG in locating the epileptic focus in children with refractory epilepsy? 2. What is the clinical efficacy of MEG in identifying epileptic foci? Participants will: 1. Be divided into 2 groups: the case group and the control group. Participants in the case group will undergo both MEG and SEEG/ECoG for preoperative assessment, while patients in the control group will undergo only SEEG/ECoG before surgery. 2. Be followed up at 1, 3, 6, and 12 months after surgery to assess seizure control, neurological function, and quality of life.

This description comes directly from the study's public registry record.

Talk to the study team

Ye Song, Medical Doctor  ·  +86-020-81886332  ·  15625984282@163.com

Always discuss trial participation with your own doctor first.

Locations (1)

Guangzhou Women and Children's medical centerGuangzhou, Guangdong, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07064421