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A real world study of the myopia control effect of YEKA defocusing lenses

A real world study of the myopia control effect of YEKA defocusing lenses

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500095413
Enrollment
Unknown
Registered
2025-01-07
Start date
2025-02-10
Completion date
Unknown
Last updated
2025-01-13

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

Conditions

Myopia

Interventions

great controlled group:Wear an YEKA- great controlled defocusing lens
great vision group:Wear an YEKA- great vision defocusing lens

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
7 Years to 12 Years

Inclusion criteria

Inclusion criteria: (1) Ages 7-12 (2) SER: -1.00 to -5.00 diopter (D) (3) Astigmatism and anisometropia were =1.50D (4) The best corrected visual acuity (VA) in one eye is 1.0 or better

Exclusion criteria

Exclusion criteria: (1) Shallow anterior chamber or intraocular pressure > 21mmHg; (2) Suffering from eye diseases such as keratitis, pink eye, acute inflammation around the eye, and glaucoma; (3) strabismus or binocular abnormalities; (4) wearers of contact lenses (including those wearing contact lenses during the test); (5) Those who have used a light-feeding device in the past 3 months; (6) are using or have used myopia control means in the past 1 month, or plan to use myopia control means; (7) Patients with poor compliance who are considered inappropriate to continue to participate in the clinical trial;

Design outcomes

Primary

MeasureTime frame
Mydriatic computer diopter;Mydriatic computer diopter;Axial length;Axial length;

Countries

China

Contacts

Public ContactLongqian Liu

West China Hospital of Sichuan University

bq15651@hotmail.com+86 189 8060 1759

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026