Ireland
--:--IST
Recruiting Observational

Phenotypic Exploration of Autism Spectrum Disorders Retrospective and Prospective Data

NCT04923854 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2021-07-01
Last updated
2022-04-18

Condition(s) studied

Autism Spectrum Disorder

Investigational drug(s) / intervention(s)

No intervention

No intervention: No intervention

Study summary

Autism Spectrum Disorders (ASD) are a heterogeneous group of severe developmental abnormalities of the nervous system characterized by deficits in social interaction and verbal and nonverbal communication affecting approximately 1% of the general population.

In 5-40% of cases, genetic factors are identified as the cause of these disorders.

Despite this unique definition and the advancement of techniques, ASD is still a clinically and genetically heterogeneous condition, as several hundred genes have been identified to date.

Primary Objective and Endpoint Primary Objective:

Exploration of phenotypic heterogeneity in patients with ASD.

Primary endpoint:

* Routine Care Clinical Investigation Criteria.
* Scores on assessment scales,

Eligibility

Sex
ALL
Min age
1 Year
Max age
18 Years
Healthy volunteers
No
Inclusion Criteria: * child (age \<18 years) with Autism Spectrum DisorderAutism Spectrum Disorder Exclusion Criteria: \-

Primary outcome measure(s)

  • The main objective is to better understand the phenotypic heterogeneity of Autism Spectrum Disorder (ASD). — 12 months
    DSM5 (Diagnostic statistical Manual of Mental disorders) Autism diagnostic scales

Trial sites (1)

FacilityCityRegionStatus
Hôpital Robert Debré Paris France Recruiting
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 NCT04923854 on ClinicalTrials.gov ↗ ← All trials in France