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N/A N=10

Pediatric Language and Memory Mapping in Refractory Epilepsy Using Magnetoencephalography

Epilepsy

Enrolled (actual)
10
Serious AEs
0.0%
Results posted
Feb 2025
Primary outcome: Primary: Completed MEG — 1 participants

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
Baseline MEG Test (Diagnostic_test); Receptive Language Task (Behavioral); Memory Task (Behavioral)
Age
Pediatric, Adult · 8+ yrs
Sex
All
Sponsor
University of Arkansas
Primary completion
Jul 2022

Outcome Measures

OutcomeResultp-value
PRIMARY
Completed MEG
1

Summary

This is a pilot research study where language and working memory tasks will be used to study brain activities from children with epilepsy. Specifically for language assessment, a well-known MEG language protocol will be used and novel signal processing techniques will be applied. A widely utilized paradigm will be used to study memory function and adapt signal-processing techniques from previous literature for the processing and analysis of MEG signals collected during memory task. No treatment/intervention will be performed or evaluated in this pilot research study.

Eligibility Criteria

Inclusion Criteria

  • 8 to 21 years old
  • Drug-resistant focal epilepsy
  • Enrolled in the Arkansas Children's Neuroscience Center Comprehensive Epilepsy Program
  • Under evaluation for resective surgery
  • English speakers. This is not a treatment/intervention study.

Exclusion Criteria

  • Previous resective surgery for epilepsy
  • Presence of progressive neurodegenerative disorders
  • Presence of significant magnetic artifacts; electronic, magnetic or metallic implants (e.g. pins, screws, shrapnel remains, surgical clips, artificial heart valves, cochlear implants, vascular stents pacemakers); or permanent make-up or tattoos made with metallic dyes
  • Presence of seizures within 24 hours of the MEG
  • Use of sedation during the MEG acquisition
  • Inability to be in a seated or supine position during the tasks
  • Major medical disorders (e.g. HIV, cancer)
  • Significant visual or auditory disabilities
  • Physical disabilities that interfere with accomplishment of study tasks (when applicable)
  • Claustrophobia, or fear of cramped or confined spaces
  • Pregnancy or suspected pregnancy
  • Any condition that the investigator feels might put the patient at risk
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04888637). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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