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Study on Diagnostic Accuracy Evaluation and Oculomotor Characteristics of Amblyopia Based on Pupil.io Infrared Eye Tracker

Study on Diagnostic Accuracy Evaluation and Oculomotor Characteristics of Amblyopia Based on Pupil.io Infrared Eye Tracker

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600132318
Enrollment
Unknown
Registered
2026-09-11
Start date
2026-09-20
Completion date
Unknown
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Amblyopia

Interventions

orthotropic control group:N/A

Sponsors

Eye Hospital, Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 18 Years

Inclusion criteria

Inclusion criteria: 1.Aged 3 to 18 years, no gender restriction; 2.Clinically diagnosed amblyopia (best corrected visual acuity of the amblyopic eye less than 0.8 or meeting age-specific diagnostic criteria, interocular difference = 2 lines); 3.Amblyopia type: anisometropic, strabismic, or refractive amblyopia; 4.Able to understand and cooperate with Pupil.io infrared eye tracker examination; 5.Informed consent signed by the subject or their legal guardian.

Exclusion criteria

Exclusion criteria: 1.Manifest nystagmus affecting fixation stability assessment; 2.History of ocular surgery; 3.Coexisting ocular diseases (cataract, glaucoma, retinal diseases, optic nerve diseases, etc.); 4.Neurological disorders or developmental disabilities (autism spectrum disorder, cerebral palsy, etc.); 5.Intellectual disability or psychiatric disorders precluding cooperation with examinations; 6.Other conditions deemed unsuitable by the investigators.

Design outcomes

Primary

MeasureTime frame
log BCEA;

Secondary

MeasureTime frame
Binocular coordination;Fixation stability;Saccadic function;Smooth pursuit gain;

Countries

China

Contacts

Public ContactYe Xinjie

Eye Hospital, Wenzhou Medical University

405780447@qq.com+86 571 88185666

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Sep 19, 2026