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Early Determinants of Multidimensional Outcome at School Age After Neonatal Arterial Ischemic Stroke

C

Centre Hospitalier Universitaire de Saint Etienne

Status

Completed

Conditions

Cerebral Infarction

Study type

Observational

Funder types

Other

Identifiers

NCT02511249
1008026
ANSM (Other Identifier)

Details and patient eligibility

About

While perinatal ischemic stroke is the most frequent form of childhood stroke, early determinants of outcome remain poorly understood. Two main structural biases limit the accuracy of most studies: heterogeneity of the population and short follow-up.

Perinatal ischemic stroke includes several conditions that differ in pathophysiology and timing of occurrence. Yet, it is not surprising that risk factors and outcome depend primarily on the type of stroke. Age at evaluation also plays a major role after a neonatal insult. Even though the original lesion is static and focal in perinatal stroke, its consequences grow over time within the maturing brain and affect all fields of neurodevelopment.

The objective of the AVCnn study was to delineate the determinants, clinical and imaging presentation, mechanism, and long term outcome of a category of perinatal stroke (neonatal arterial ischemic stroke: NAIS). This led to the AVCnn cohort, which now gives us the opportunity to regularly monitor a large cohort of children having suffered an NAIS.

Full description

Between November 2003 and October 2006, a cohort of one hundred symptomatic term newborns with AIS confirmed through early brain imaging has been constituted.

Regular contacts with the families and their local physician have been maintained since enrollment. In 2010, families were asked through postal mail to participate in the 7 years assessment (AVCnn7ans). Those who accepted were contacted by phone by the coordinators of the study during the months preceding the child's seventh birthday and invited to attend a presentation in person of the current project. This evaluation took place face-to-face for a whole day in a medical setting close to the family residence. The evaluation team included a neuropsychologist, a speech therapist and either a pediatric neurologist or a pediatric physical and rehabilitation medicine practitioner.

Enrollment

80 patients

Sex

All

Ages

7 to 7 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Belonging to the AVCnn cohort

Exclusion criteria

  • Lost to follow-up at 7 years.
  • Refusal to participate in the current assessment.

Trial design

80 participants in 1 patient group

cohort
Description:
1 evaluation day : The evaluation team included a neuropsychologist, a speech therapist and either a pediatric neurologist or a pediatric physical and rehabilitation medicine practitioner. tests carried out : Global intellectual functioning (WISC-IV), Oral language (N-EEL), Gross and fine motor abilities (clinical examination, Box \& Block test, 9 Hole Peg test)

Trial contacts and locations

5

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Data sourced from clinicaltrials.gov

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