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Clinical Trials in France / NCT06928727
Recruiting Observational

Ocular Characteristics in Patients With Craniosynostosis

NCT06928727 · tracked via the Priya Life Science France tracker
Sponsor
Centre Hospitalier Universitaire, Amiens
Phase
Observational
Started
2025-04-04
Last updated
2026-02-12

Condition(s) studied

CraniosynostosisStrabismusIntracranial HypertensionAmblyopia

Study summary

Craniosynostosis are cranial deformations due to the premature closure of one or more cranial sutures. These deformations affect approximately one in 2.500 births. In most cases, craniosynostoses are isolated with unknown (non syndrome). On the other hand, 20% of these deformations are associated with other concentration (syndrome).

Craniosynostosis has morphological (associated dysmorphism) and functional (growth conflict between the skull and the brain) repercussions. Ophthalmological disorders are frequent: refractive disorders, oculomotor disorders, optic nerve damage, sensory damage.

This retrospective study aims to describe the ocular clinical characteristics associated with craniosynostosis in patients followed at the Amiens University Hospital.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Diagnosis of craniostenosis Exclusion Criteria: * Posterior plagiocephalia

Primary outcome measure(s)

  • Rate of strabismus and amblyopia — 6 months
    Rate of strabismus and amblyopia

Trial sites (1)

FacilityCityRegionStatus
CHRU Amiens Amiens France Recruiting

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Other trials for the same condition

Strategies for Weaning From External Ventricular Drainage Starting soon
Early Detection and Prevention of Amblyopia and Visual Impairment Through Systematic Pediatric Vision Screening Starting soon
Network Of Clinical Research Studies On Craniosynostosis, Skull Malformations With Premature Fusion Of Skull Bones Active, not recruiting
Assessment of Venous Drainage in Idiopathic Intracranial Hypertension Active, not recruiting
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 NCT06928727 on ClinicalTrials.gov ↗ ← All trials in France