Exploring treatments for amblyopia in children using OCT technology
Official title: OCT Eccentric Fixation, Fixation Stability, and Amblyopia in Children
Run by State University of New York College of Optometry · NCT05714449 · Data updated 2026-11-12
This study is testing different treatments for amblyopia in children aged 4-16 to see how well they improve vision using eye patches and foveation therapy.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 4 Years to 16 Years |
| Sex | All |
| Enrollment | 30 (estimated) |
| Sponsor | State University of New York College of Optometry Academic / other |
| Locations | 1 site (New York, New York) |
| Status | Recruiting |
| Started | January 25, 2023 |
| Main results expected | February 24, 2027 |
| Study ends | March 24, 2027 |
| Registry record updated | October 8, 2026 |
| Trial ID | NCT05714449 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are children aged 4-16 with amblyopia characterized by specific visual acuity and ocular conditions.
✕Probably not a fit
Patients with amblyopia not meeting the inclusion criteria or those with other ocular conditions may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study investigates the relationship between OCT eccentric fixation and various treatment methods for amblyopia in children. It aims to assess changes in fixation eye movement and macular sensitivity following patching treatment and foveation therapy over a 12-week period. The study will enroll children aged 4-16 with specific types of amblyopia, utilizing interventions such as eye patches and foveation therapy to evaluate their effectiveness. The outcomes will help to better understand how these treatments impact visual function in affected children.
Why it matters
Potential benefit: If successful, this study could lead to improved treatment strategies for amblyopia, enhancing visual outcomes in children.
How similar studies have gone: While there have been studies on amblyopia treatments, the specific use of OCT eccentric fixation in this context is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. children with best-corrected visual acuity (BCVA) of 20/40 (equivalent to 0.3 logMAR) or worse in the amblyopic eye (ranging from 20/40 to 20/400), and interocular difference of BCVA was at least two logMAR lines, 2. ocular causes of amblyopia that were identified as refractive(i.e., anisometropic, strabismus, or strabismic-anisometropic. * Anisometropia included interocular difference of spherical equivalent \>=1D or interocular difference of astigmatism cylinder magnitude \>=1D; * strabismus included those with deviation \>=10PD or good alignment after prior strabismus surgery; * combined type included those who meet the criteria of both anisometropia and strabismus. * For the patching group, we will enroll 15 children with strabismic amblyopia who are prescribed patching treatment. Age: 4-12 years old. * For the foveation therapy group, we will enroll 15 children with strabismic amblyopia who are prescribed foveation therapies. Age: 8-16 years old. Exclusion Criteria: * born before 32 weeks gestational age; * neurologic, developmental, or systemic illnesses known to be associated with ocular pathologies; * congenital or acquired macular pathology.
Where it's running
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SUNY College of Optometry
New York, New York, United States Recruiting
Study contacts
- Principal investigator: Jingyun Wang — SUNY College of Optmetry
- Study coordinator: Jingyun Wang, PhD
- Email: jwang@sunyopt.edu
- Phone: 2129385759
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.