Observing eye growth in children with myopia
Evolution of Ocular Growth in Myopic Children: A Prospective Cohort Study
This study looks at how myopia, or nearsightedness, changes in children in France to help find better ways to prevent it.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 1000 (estimated) |
| Ages | 6 Years to 17 Years |
| Sex | All |
| Sponsor | Fondation Ophtalmologique Adolphe de Rothschild Research network |
| Locations | 1 site (Paris) |
| Trial ID | NCT06895044 on ClinicalTrials.gov |
What this trial studies
This study aims to observe the evolution of ocular growth in children diagnosed with myopia, a common vision condition. It will involve a cohort of myopic children in Europe, particularly focusing on those in France, to collect high-quality retinal and corneal images through ophthalmological follow-ups. The goal is to better understand how myopia progresses in this population, as current research is limited and primarily conducted in Asia. By gathering detailed imaging and data, the study hopes to contribute valuable insights into effective preventive strategies for myopia.
Who should consider this trial
Good fit: Ideal candidates for this study are children with myopia in at least one eye, defined as a refractive error of -0.50 diopters or worse.
Not a fit: Patients with eye trauma, inflammatory conditions, or a history of intraocular surgery in both eyes may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved understanding and management of myopia in children, potentially reducing the risk of severe visual impairment.
How similar studies have performed: While there is limited research on ocular growth in myopic children in Europe, studies in Asia have shown promising results in understanding myopia progression.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Myopia in at least one eye, defined as a refractive error in spherical equivalent ≤ -0.50 diopters (autorefraction under cycloplegia) * Affiliated or beneficiary of a social security system * Explicit consent from a holder of parental authority Exclusion Criteria: * Presence of trauma in both eyes * Presence of inflammatory conditions in both eyes * History of intraocular surgery (cataract, filtering surgery, intra-vitreal surgery) in both eyes * Patient benefiting from legal protection measures
Where this trial is running
Paris
- Hôpital Fondation A. de Rothschild — Paris, France (Recruiting)
Study contacts
- Principal investigator: Thibaut Chapron, Dr — Hôpital Fondation Adolphe de Rothschild
- Study coordinator: Amelie Yavchitz
- Email: ayavchitz@for.paris
- Phone: +33148036454
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.