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Evaluating the myopia control effect of multi-ring defocus lenses in children with different degrees of heterophoria and myopia

Evaluating the myopia control effect of multi-ring defocus lenses in children with different degrees of heterophoria and myopia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500099686
Enrollment
Unknown
Registered
2025-03-27
Start date
2025-03-27
Completion date
Unknown
Last updated
2025-03-31

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

Conditions

Myopia

Interventions

Experimental Group:Multi-ring defocus lenses
Control Group:Ordinary lense

Sponsors

The Zhongshan Ophthalmic Center,Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
8 Years to 13 Years

Inclusion criteria

Inclusion criteria: 1.Age 8-13 years old, male or female; 2.Binocular spherical equivalent -1.00 to -5.00D; 3.Astigmatism <=-1.50D in both eyes; 4.Anisometropia <=1.00D; 5.The best corrected visual acuity of both eyes was not less than 20/20; 6.Strabismus should not exceed 20 degrees; 7.Good cognition and ability to cooperate with the examination; 8.Able to consent and participate in the follow-up study; 9.Signed informed consent.

Exclusion criteria

Exclusion criteria: 1.Limited activity due to a medical illness, drug or emotional state; 2.Patients with organic diseases of eye and other parts; 3.Patients with a history of eye surgery; 4.The use of other drugs that may affect vision (except for cycloplegic agents for examination); 5.Have worn contact lenses within the last month; 6.Those who have used other myopia prevention and control methods in the past year (such as other defocusing lenses, progressive lenses, bifocal lenses, bifocal prisms, orthokeratology lenses, defocusing soft lenses, defocusing RGP, atropine, etc.); 7.Other investigators involved in the past month that may directly or indirectly affect clinical outcomes; 8.Subjects who are unable to communicate or do not follow instructions; 9.Other conditions in which the investigator deems it inappropriate to participate in a clinical trial.

Design outcomes

Primary

MeasureTime frame
Axial Length;

Secondary

MeasureTime frame
Spherical equivalent;

Countries

China

Contacts

Public ContactJinrong Li

The Zhongshan Ophthalmic Center,Sun Yat-sen University

lijinrong@gzzoc.com+86 13763312661

Outcome results

None listed

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