Effect of Light-Blocking Lenses on Hyperopic Anisometropic Children (NCT07142928) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Effect of Light-Blocking Lenses on Hyperopic Anisometropic Children
China90 participantsStarted 2025-08-25
Plain-language summary
To evaluate the effectiveness of light-blocking lenses in promoting emmetropization and reducing anisometropia in children with hyperopic anisometropia, and to assess the impact of light-intercepting lenses on visual function in this population.
Who can participate
Age range6 Years – 12 Years
SexALL
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Inclusion Criteria:
* Aged 6 years or older and 12 years or younger;
* The more hyperopic eye has a spherical refractive error between +3.0 D and +7.5 D; the less hyperopic eye has a spherical refractive error of at least +2.0 D; cylindrical refractive error between -2.0 D and 0 D; interocular difference in spherical power \>=1.5 D and in cylindrical power \<=1.0 D;
* Best-corrected visual acuity of 0.0 logMAR or better in both eyes;
* Ocular deviation with spectacles less than 10 prism diopters;
* Has been wearing standard single-vision spectacles regularly for more than six months;
* In good general health, capable of receiving the study intervention, and willing to comply with the study protocol;
* Written informed consent obtained from both the parent/guardian and the child, with agreement to comply with all study procedures and maintain follow-up availability throughout the study period;
Exclusion Criteria:
* History of ocular trauma or eye surgery;
* Presence of pathological abnormalities on anterior or posterior segment examination, or a history of organic ocular diseases such as cataract, glaucoma, corneal disease, or fundus disorders;
* Intraocular pressure greater than 21 mmHg;
* Presence of systemic diseases or other conditions deemed unsuitable for study participation;
* Any other condition deemed inappropriate for participation in the clinical trial by the investigator;
What they're measuring
1
Axial length
Timeframe: At baseline, 6 months, and 12 months
Trial details
NCT IDNCT07142928
SponsorZhongshan Ophthalmic Center, Sun Yat-sen University