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To assess the effectiveness and safety of asymmetrical peripheral defocus lenses for delaying the progression of myopia in children

To assess the effectiveness and safety of asymmetrical peripheral defocus lenses for delaying the progression of myopia in children

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500107298
Enrollment
Unknown
Registered
2025-08-07
Start date
2021-09-22
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

myopia

Interventions

Experimental group:Refractive correction is performed using asymmetrical peripheral defocus lenses
Control group:Refractive correction is performed with single vision lenses

Sponsors

Zhongshan Ophthalmic Center, Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
8 Years to 13 Years

Inclusion criteria

Inclusion criteria: 1. Ages 8-13 years, male or female; 2. Myopia equivalent spherical power -1.00~-5.00D; 3. Astigmatism<=-1.50D; 4. Ansometropia<=1.00D; 5. Best corrected visual acuity not less than 20/20; 6. Strabismus does not exceed 20? 7. Good cognition and ability to cooperate with the examination; 8. Able to consent and participate in follow-up studies; 9. Sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Restricted activity due to medical illness, medication, or emotional state; 2. Patients with organic diseases of the eyes and other parts; 3. Those with a history of previous eye surgery; 4. Those who are concomitant with other drugs that may affect vision; 5. Those who have worn contact lenses in the past month; 6. Those who have used other myopia prevention and control methods in the past year (such as other defocal lenses, gradual Lenses, bifocals, bifocal prisms, orthokeratology lenses, defocus soft lenses, defocus RGP, atropine, etc.); 7. Participation in other studies that may directly or indirectly affect clinical outcomes within the past month He who; 8. Subjects who are unable to communicate or do not follow instructions; 9. Other conditions that the investigator considers inappropriate to participate in clinical trials.

Design outcomes

Primary

MeasureTime frame
Equivalent spherical power;Axial length;

Countries

China

Contacts

Public ContactLi Jinrong

Zhongshan Ophthalmic Center, Sun Yat-sen University

lijingr3@mail.sysu.edu.cn+86 137 6331 2661

Outcome results

None listed

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