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NCT07387159

Effect of MiYOSMART iQ Spectacle Lenses on Myopia Progression in Children

Recruiting now NA Last updated 6 February 2026
What this trial tests

NA trial testing MiYOSMART iQ spectacle lenses in Myopia, Child Myopia Progression in 70 participants. Currently enrolling.

Timeline
4 February 2026
Primary endpoint
31 December 2026
28 February 2027

Quick facts

Lead sponsorHoya Lens Rus LLC
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationnon randomized
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment70
Start date4 February 2026
Primary completion31 December 2026
Estimated completion28 February 2027
Sites1 location across Russia

Drugs / interventions tested

Conditions studied

Sponsor

Hoya Lens Rus LLC

Who can join

Adults 8 to 11, any sex, with Myopia, Child Myopia Progression. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This prospective, single-center study aims to evaluate the efficacy and safety of MiYOSMART iQ spectacle lenses with DIMS (Defocus Incorporated Multiple Segments) and Triple Enhanced Design (TED) technology in slowing myopia progression in children aged 8-11 years. 35 children with myopia (spherical equivalent -0.5 to -6.0 D) will be prescribed MiYOSMART iQ lenses and followed for 6 months. The study will compare changes in spherical equivalent refraction and axial length against a historical control group (n=35) using ANCOVA. Secondary outcomes include measurements of peripheral refraction and contrast sensitivity at the first prescription. The study hypothesis is that wearing MiYOSMART iQ lenses for 6 months significantly slows myopia progression compared to single-vision spectacle correction.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07387159.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing