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NCT07387159
Effect of MiYOSMART iQ Spectacle Lenses on Myopia Progression in Children
NA trial testing MiYOSMART iQ spectacle lenses in Myopia, Child Myopia Progression in 70 participants. Currently enrolling.
31 December 2026
Quick facts
| Lead sponsor | Hoya Lens Rus LLC |
|---|---|
| Phase | NA |
| Status | Recruiting now |
| Study type | INTERVENTIONAL |
| Allocation | non randomized |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 70 |
| Start date | 4 February 2026 |
| Primary completion | 31 December 2026 |
| Estimated completion | 28 February 2027 |
| Sites | 1 location across Russia |
Drugs / interventions tested
- MiYOSMART iQ spectacle lenses
Conditions studied
- Myopia, Child Myopia Progression — all drugs for Myopia, Child Myopia Progression →
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.
Verify or expand the search:
- PubMed search for NCT07387159
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Related trials
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT07387159 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Hoya Lens Rus LLC
- Last refreshed: 6 February 2026
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