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NCT04638452Recruiting

Evaluation of Behavioural Psycho & Physiological Responses in People With ASD During a Blood Test in Routine Care Practice

Evaluation of Behavioural, Psychological and Physiological Responses in People With Autism Spectrum Disorder (ASD) During a Blood Test in Routine Care Practice

Source: ClinicalTrials.gov · Last updated 16 Mar 2026

Brief summary (registry, in English)

The project is a prospective study designed to characterize behaviour and its psycho-physiological correlates of participants with ASD (children and adults) in comparison with subjects without ASD matched in age during blood test in common practice.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
150 (estimated)
First submitted
15 Oct 2020
Start date
8 Feb 2021
Primary completion date
30 Nov 2026
Lead sponsor
Centre Hospitalier Charles Perrens, Bordeaux
Diseases
Autism
NCT number
NCT04638452

What you commit to

  • Study type: Interventional
  • Planned participants: 150
  • From 8 Feb 2021 to the primary completion date, 30 Nov 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Person with unstabilized drug therapy
  • Person with pathology or receiving a treatment which can have an impact in modification of the pain

Other illness

  • Person with oculomotor and/or neuro-motor disorders

Other

  • All participants :
  • Person with acute or chronic pain
  • Pregnant or breastfeeding woman
  • Person with deprivation of liberty
  • Person who no consent to participate in the study or no consent to realised video recording
    • Participants without ASD :
  • Protected adult
  • Person with ASD diagnosis

Who the study is looking for

  • All participants :
  • Person over 6 years of age
  • Person who consent to participate in the study
  • Membership of the social security scheme
  • Person who not received analgesic treatment that may interfere with pain perception
  • Person with medical prescription for blood sample
    • Participants with ASD :
  • Person with ASD diagnosis
  • If applicable, legal authority consent to participate in the study

Age in the registry: 6 years to 65 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Centre Hospitalier Charles Perrens
Coordinator of this site? Confirm its status
BordeauxFranceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.