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Efficacy and Safety of Eyetronix Flicker Glasses to the Treatment of Anisometropic Amblyopia

Efficacy and Safety of Eyetronix Flicker Glasses to the Treatment of Anisometropic Amblyopia in Chinese Children

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02970708
Enrollment
176
Registered
2016-11-22
Start date
2017-01-31
Completion date
2020-01-31
Last updated
2016-11-22

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

Conditions

Amblyopia, Anisometropic

Brief summary

To evaluate the efficacy and safety of Eyetronix Flicker Glassess therapy in treating anisometropic amblyopia.

Detailed description

A total of 176 children with anisometropic amblyopia, aged 4 to 13 years, will randomize to receive patching or Eyetronix Flicker Glasses treatment in a 1:1 ratio.Eyetronix Flicker Glasses, a lightweight spectacle frame with liquid crystal lenses that provide direct square-wave alternating occlusion, will be used at a pre-programmed temporal frequency. Patching is a traditional treatment of amblyopia. The best corrected visual acuity, contrast sensitivity, binocular function,visual evoked potential and functional MRI will be measured at baseline and follow-up visits to assess the improvement of amblyopia.Feedback information from the questionnaires will be used to evaluate the compliance and adverse effects.

Interventions

DEVICEEFG group

88 anisometropic amblyopia will be recruited to receive Eyetronix Flicker Glasses treatment.

DEVICEPatching group

88 anisometropic amblyopia will be recruited to receive patching treatment.

Sponsors

Shanghai Eye Disease Prevention and Treatment Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
4 Years to 13 Years
Healthy volunteers
No

Inclusion criteria

1. aged from 4 to 13 years old 2. the best corrected visual acuity in the amblyopic eye is no more than 0.1logMAR, with two lines or more of difference between the two eyes 3. anisometropia is defined as an inter-ocular spherical refractive error difference of 1.00 D or more or a cylindrical difference of 1.50 D or more. 4. no amblyopia treatment one month prior to the study except refractive correction. 5. myopia is less than -6.00D or hyperopia is less than +9.00D, strabismus was less than 20 prism diopters 6. willing to participate in this study and be able to follow up on time

Exclusion criteria

1. ocular disease and other disease that have an influence on the visual acuity 2. history of ocular surgery that have an influence on the visual acuity 3. the patient is receiving other amblyopia treatment except refractive correction 4. a family or personal history of seizures 5. the patient is using some medicine that may have an influence on visual acuity

Design outcomes

Primary

MeasureTime frameDescription
best corrected visual acuity6 monthshave an improvement of best corrected visual acuity in the amblyopic eyes

Secondary

MeasureTime frameDescription
stereocuity6 monthshave an improvement of stereocuity in the amblyopic eyes
contrast sensitivity function6 monthshave an improvement of contrast sensitivity in the amblyopic eyes
visual evoked potential6 monthsP100 latency decrease and N75-P100 amplitude increase in the amblyopic eye.
functional MRI6 monthsthe visual cortex activity have an improvement
best corrected visual acuitya year and a halfhave an improvement of best corrected visual acuity in the amblyopic eyes

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026