Actively Recruiting

Age: 3Years - 18Years
All Genders
NCT07064421

Non-Helium Magnetoencephalography in Pediatric Refractory Epilepsy

Led by Guangzhou Women and Children's Medical Center · Updated on 2025-07-14

100

Participants Needed

1

Research Sites

164 weeks

Total Duration

On this page

Sponsors

G

Guangzhou Women and Children's Medical Center

Lead Sponsor

B

Beijing X-Magtech Technology Limited

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Non-Helium Magnetoencephalography in Pediatric Refractory Epilepsy

Who Can Participate

Age: 3Years - 18Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 3 and 18 years old
  • Diagnosed with refractory epilepsy
  • Able to cooperate with magnetoencephalography evaluation and recording
Not Eligible

You will not qualify if you...

  • Serious comorbidities or neurological or psychiatric disorders affecting magnetoencephalography
  • Use of drugs that affect central nervous system function
  • Not suitable for surgical procedures
  • Progressive neurological disorders

AI-Screening

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Trial Site Locations

Total: 1 location

1

Guangzhou Women and Children's medical center

Guangzhou, Guangdong, China, 511399

Actively Recruiting

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Research Team

Y

Ye Song, Medical Doctor

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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