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Clinical Trials in France / NCT06442592
Recruiting Not applicable

Characterization and Support for Neurodevelopmental Disorders Associated With Congenital Heart Defects

NCT06442592 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2024-07-08
Last updated
2026-04-03

Condition(s) studied

Congenital Heart DefectsNeurodevelopmental Disorder

Investigational drug(s) / intervention(s)

Blood samplingAssessment of neurodevelopment (CA)Assessment of neurodevelopment (Nantes)Assessment of the parental stress

Blood sampling: An EDTA blood sample will be taken from the children and their two parents. Sample volume will be 2 x 3mL.

Assessment of neurodevelopment (CA): The children will be seen by a neuropsychologist, who will then determine whether or not they have neurodevelopmental disorders.

Assessment of neurodevelopment (Nantes): The children will be seen by a multidisciplinary team (including a neuropsychologist), who will then determine whether or not they have neurodevelopmental disorders.

Assessment of the parental stress: Parents' parental stress will be assessed using the Parental Stress Index (PSI) questionnaire.

Study summary

The leading cause of birth defects, Congenital Heart Defects (CHD) affect 12 million people worldwide and 41,000 newborns/year in Europe. It's a major cause of life-long morbidity and mortality, and a crucial public health issue. More than 50% of childs born with critical CHD will develop Neurodevelopmental Disorders (NDs), requiring specific care and impairing quality of life. NDs corresponds to early and lasting disturbances in cognitive, affective and behavioral development, linked to abnormalities in brain development. They are heterogeneous, affecting language, learning, motor skills, intellectual efficiency, social cognition, attention, memory and executive functions, and are associated with psychosocial difficulties (adaptive behavior, social interactions). This hidden handicap is the main long-term sequels of CHD, even before cardiovascular sequels, in individuals who often underwent multiple heart operations in early childhood. NDs concern not only complex CHD, but also simple CHD repaired in childhood and considered cured.

The origin of TND associated with CHD is largely unknown. To date, few genetic or environmental causes have been clearly identified, but recent work has suggested that a common origin may link cardiac malformation and neurodevelopmental abnormality.

The CATAMARAN - Pediatrics project is designed to detect potential neurodevelopmental delays associated with CHD as early as age 3, and to identify individual susceptibility factors involved in the occurrence of NDs in CHD children.

Eligibility

Sex
ALL
Min age
3 Years
Max age
11 Years
Healthy volunteers
No
Inclusion Criteria: * Child (aged 3 to 11) with critical MCC operated on for heart surgery during the first three months of life * Parents and child affiliated with or benefiting from a social security or similar scheme * Parents' and child's good understanding of the French language * Free, informed and written consent of both parents for themselves and for the child * Free, informed and written consent of the child aged 6 and over * Biological parents Exclusion Criteria: * Genetic anomaly or malformative syndrome associated with neurodevelopmental abnormalities, identified prior to inclusion * Neurodevelopmental assessment not practicable

Primary outcome measure(s)

Trial sites (5)

FacilityCityRegionStatus
Chu Brest Brest Brittany Region Recruiting
CHU Rennes Rennes Brittany Region Recruiting
CHU Nantes Nantes Loire-Atlantique Recruiting
CHU Angers Angers Maine-et-Loire Recruiting
CHU Tours Tours Val de Loire Recruiting

More Nantes University Hospital trials in France

Other trials for the same condition

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 NCT06442592 on ClinicalTrials.gov ↗ ← All trials in France