Autism Spectrum Disorder Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
For patients with autism:
- You must already be enrolled in a related study called "C16-89 – Study of genetic factors involved in ASD and related disorders"
- You must have a confirmed diagnosis of Autism Spectrum Disorder (ASD) based on recognised international guidelines, assessed by a specialist using standard diagnostic tools
- You must be at least 24 months (2 years) old
- You must be covered by French health insurance
- You (or your legal guardian, if you are under 18 or under legal protection) must have signed a consent form agreeing to take part
For family members (relatives) of patients:
- You must already be enrolled in the related study "C16-89"
- You must be at least 24 months (2 years) old
- You must be covered by French health insurance
- You (or your legal guardian, if applicable) must have signed a consent form
For healthy volunteers (controls):
- You must already be enrolled in the related study "C16-89"
- You must be at least 24 months (2 years) old
- You must be covered by French health insurance
- You (or your legal guardian, if applicable) must have signed a consent form
Who may not be able to join:
For everyone:
- People with very severe intellectual disability (very low IQ or a developmental age below 18 months)
- People with a medical or psychiatric condition that makes joining the study unsuitable (confirm with trial site)
- People who cannot have an MRI scan for medical reasons (for example, having a metal implant)
- People who are currently pregnant or breastfeeding
- People who do not wish to be told if an unusual finding is discovered in their brain scan
For family members (relatives) only:
- If genetic testing reveals that a family relationship does not exist as expected (confirm with trial site)
For healthy volunteers (controls) only:
- People with a history of neurological conditions (except intellectual disability)
- People with a personal history of certain conditions, including: schizophrenia, addiction, bipolar disorder, repeated episodes of depression, severe or unstable anxiety, epilepsy, or significant inflammatory disease requiring immune-suppressing medication
For patients only:
- If your autism diagnosis cannot be confirmed by the assessments carried out after joining the study
For everyone:
- If a reason that prevents a safe MRI scan is discovered during the scan itself (for example, claustrophobia)
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Richard Delorme, M.D, Ph.D, APHP, France
Phone: +33140032002
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
3DT1 MRI derived variables; Resting state fMRI derived variables; Task based fMRI derived variables; Diffusion MRI derived variables; quantitative T1 and quantitative T2 MRI
Can't join this trial?
Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.