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Recruiting NCT06816446

NCT06816446 Influence of Rodenstock Spectacle Lenses on Myopia Progression.

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Clinical Trial Summary
NCT ID NCT06816446
Status Recruiting
Phase
Sponsor Rodenstock GmbH
Condition Myopia
Study Type INTERVENTIONAL
Enrollment 185 participants
Start Date 2025-07-22
Primary Completion 2026-12

Trial Parameters

Condition Myopia
Sponsor Rodenstock GmbH
Study Type INTERVENTIONAL
Phase N/A
Enrollment 185
Sex ALL
Min Age 6 Years
Max Age 12 Years
Start Date 2025-07-22
Completion 2026-12
Interventions
Myopia control spectacle lensSingle-vision lens

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Brief Summary

The prevalence of myopia in Singapore is among the highest in the world, with 65 percent of our children being myopic by Primary 6, and 83 percent of young adults being myopic. As such, Singapore is often labelled as the "Myopia Capital of the World". By 2050, it is projected that 80 to 90 per cent of all Singaporean adults above 18 years old will be myopic and 15 to 25 percent of these individuals may have high myopia. High myopia (spherical equivalent refraction ≤ -5 D) puts one at risk of many eye disorders later in life, such as early cataracts, glaucoma and macular degeneration. These complications often cause significant morbidity and may even be sight-threatening. Hence there is an urgent and growing need for synergistic efforts to counter myopia. The goal of this clinical trial is to test the efficacy of spectacle lenses in controlling the progression of myopia in children (aged 6-12 years) over a period of 2 years. In addition, this trial aims to evaluate the impact of these spectacle lenses on central visual performance and visual comfort. Therefore, in this randomised, double-masked clinical trial, one hundred and eighty-five (n=185) subjects aged 6-12 years with mild or moderate myopia (\< -5D) will be randomised in a 1:1 allocation ratio into three strata defined by age 6-8, 8-10 and 10-12 years to ensure age balance between the two arms (control group - single vision lenses and intervention group - myopia control lenses, gender matched). In the control group, after one year (12 months) of wearing single vision lenses, the children will switch to the myopia control lenses (crossover design).

Eligibility Criteria

Inclusion Criteria: * All myopic children aged 6-12 years old * Treatment naïve * Sphere: -0.5 D till -5.00 D * Anisometropia \< 1.5D * Astigmatism \> -1.5D * Monocular best corrected visual acuity +0.1 logMAR or better, and binocular visual acuity 0.0 logMAR or better Exclusion Criteria: * On current myopia control treatments * Any diagnosed ocular conditions besides myopia or astigmatism. * No diagnosed ocularmotor conditions (Nystagmus, strabismus, etc.) * Any diagnosed chronic physical or mental disabilities * Contraindication in cycloplegia (high IOP, etc.) * Corneal astigmatism \> 1.5 D; irregular astigmatism

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