Ireland
--:--IST
Latest
Astellas Expands Its 330 Million Euro Tralee Biopharma Facility with a Second Aseptic Filling Line to Double Drug-Product Capacity Xeolas Pharmaceuticals Opens 158,000 Sq Ft State-of-the-Art Baldoyle Facility to Scale Specialty Medicine Manufacturing Priya Life Science Partners with Fleming for the 9th Annual Corporate Compliance & Transparency in Life Sciences Summit in Zurich Ireland Has the Capital and the Lessons: Digital Project Management Is How They Become Delivery Dunbar Pharma Brings First Plant-Derived Dronabinol API to UK Market Through IPS Pharma Leveraging Priya Life Science as a Data Tracker: The Ultimate Use Case & Career Guide The €100K Reality Check: Why a Six-Figure Pharma Salary in Ireland Feels Different Than in Switzerland or Germany Ireland's €93.8 Billion Non-EU Pharma Export Engine: Trade Data, Destination Markets, and Economic Impact Astellas Expands Its 330 Million Euro Tralee Biopharma Facility with a Second Aseptic Filling Line to Double Drug-Product Capacity Xeolas Pharmaceuticals Opens 158,000 Sq Ft State-of-the-Art Baldoyle Facility to Scale Specialty Medicine Manufacturing Priya Life Science Partners with Fleming for the 9th Annual Corporate Compliance & Transparency in Life Sciences Summit in Zurich Ireland Has the Capital and the Lessons: Digital Project Management Is How They Become Delivery Dunbar Pharma Brings First Plant-Derived Dronabinol API to UK Market Through IPS Pharma Leveraging Priya Life Science as a Data Tracker: The Ultimate Use Case & Career Guide The €100K Reality Check: Why a Six-Figure Pharma Salary in Ireland Feels Different Than in Switzerland or Germany Ireland's €93.8 Billion Non-EU Pharma Export Engine: Trade Data, Destination Markets, and Economic Impact
Starting soon Observational

Identification of Early Biomarkers of Pre-school ADHD

NCT07440992 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2026-03-01
Last updated
2026-02-27

Condition(s) studied

ADHD

Study summary

ADHD affects around 5% of children and manifests itself as hyperactivity, attention difficulties and motor control and balance problems. The prevalence of ADHD is particularly high in certain populations, affecting up to 25-30% of children born prematurely and around 20% of children with neurological conditions such as epilepsy. This disorder is officially diagnosed from the age of 6, according to current criteria. However, its clinical manifestations appear much earlier, having a significant impact on all aspects of the child's life, particularly in the most severe forms, which are often unrecognised due to a lack of clinical resources, and therefore without appropriate treatment.

The creation of a platform dedicated to children at risk of ADHD will enable specific clinical expertise to be developed, with the aim of proposing early targeted interventions and positively influencing the development of their trajectory. This platform will also aim to develop new diagnostic methods, based on indirect measures of attentional and executive processes, balance and the development of a risk measurement scale. This development is essential, as the assessment tools currently available lack specificity.

In order to demonstrate the reliability of the innovative diagnostic methods proposed, a comparative pilot study between children from the first clinical cohort (N=30) and a group of healthy children of the same age (N=30) will be carried out. This will enable us to study the discrimination of our tools and make any necessary adjustments. This pilot study also includes a longitudinal re-evaluation, at 12 months, of the children in the ADHD cohort, in order to study changes in these biomarkers over time.

Eligibility

Sex
ALL
Min age
3 Years
Max age
5 Years
Healthy volunteers
Accepted
Inclusion Criteria: * For ADHD subjects: * Children aged between 3.0 and 5 years and 11 months, with clinical criteria for ADHD, according to DSM 5. * Children followed in the Child and Adolescent Psychiatry Department of Robert Debré Hospital. * Children naïve to pharmacological treatment for ADHD For control subjects: * Children between 3.0 - 5 years and 11 months * No known condition or disease affecting development and behavior Exclusion Criteria: * For both groups * Intellectual disability according to DSM 5 +- WPPSI IV \< 70 * Refusal of the child or one of his parents or representatives of parental authority. * Patient under AME or not affiliated to a social security scheme

Primary outcome measure(s)

  • Scores obtained in eye tracking tests between the ADHD group and the control group (fixation duration) — At baseline
    Identification of biomarkers of visual attention by comparing scores obtained in eye-tracking tests between the ADHD group and the control group.
  • Scores obtained in eye tracking tests between the ADHD group and the control group (latencies) — At baseline
    Identification of biomarkers of visual attention by comparing scores obtained in eye-tracking tests between the ADHD group and the control group
  • Scores obtained in eye tracking tests between the ADHD group and the control group (number of errors) — At baseline
    Identification of biomarkers of visual attention by comparing scores obtained in eye-tracking tests between the ADHD group and the control group

Trial sites (1)

FacilityCityRegionStatus
Robert Debré Hospital Paris France
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 NCT07440992 on ClinicalTrials.gov ↗ ← All trials in France