Phenotypic Exploration of Autism Spectrum Disorders Retrospective and Prospective Data
Recruiting now
Conditions studied: Autism Spectrum Disorder
In brief
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,
Key facts
- Study ID
- NCT04923854
- Run by
- Assistance Publique - Hôpitaux de Paris
- People needed
- 1500
- Starts
- 2021-07-01
- Expected to finish
- 2027-07-01
- Last updated by the study team
- 2022-04-18
Who can join
Age: 1 and older, up to 18. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- child (age <18 years) with Autism Spectrum DisorderAutism Spectrum Disorder
Where it is running
- Hôpital Robert Debré — Paris, France (enrolling)
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.