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Starting soon Observational

EEG As a Genetic Selection Lever in Autism Spectrum Disorder

NCT07891065 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2026-09
Last updated
2026-10-23

Condition(s) studied

Autism Spectrum Disorder (ASD

Investigational drug(s) / intervention(s)

Collection of routine care data

Collection of routine care data: Clinical, EEG and genetic data from the patient records of the children included will be collected

Study summary

Autism Spectrum Disorder (ASD) is a growing public health concern, with genetic causes identified in about 20% of cases. While exome/genome sequencing is powerful, its cost and limited yield call for better patient selection.

Electroencephalography (EEG) shows promise: early EEG patterns can predict ASD, and specific EEG features may help identify subgroups more likely to have a genetic cause. This project explores using EEG to optimize genetic testing strategies in ASD.

Eligibility

Sex
ALL
Min age
12 Months
Max age
17 Years
Healthy volunteers
No
Inclusion Criteria: * Age \< 18 years * Children with ASD * Having undergone exome sequencing * Having undergone a sleep EEG Exclusion Criteria: * Children whose legal representative has objected to the reuse of their data * Presenting with another previously identified cause that may explain the ASD (toxic, infectious, perinatal distress)

Primary outcome measure(s)

  • EEG profil — At Baseline
    The EEG characteristics will be described according to 3 categories: 1) spike-wave bursts (SWB) profile, 2) alteration of sleep spindles profile, 3) others profile. This assessment will be conducted in a blinded manner by 3 pediatric neurologists. The analysis will focus on the first 10 minutes of sleep, using a standardized assessment grid.

Trial sites (2)

FacilityCityRegionStatus
Cabinet de Neurologie Pédiatrique Le Ban Saint-Martin France
CHR Metz-Thionville Hopital Femme Mere Enfant Metz France

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07891065 on ClinicalTrials.gov ↗ ← All trials in France