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Evaluation of the effectiveness of peripheral defocusing lenses for myopia progression

Evaluation of the effectiveness of peripheral defocusing lenses for myopia progression

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500102397
Enrollment
Unknown
Registered
2025-05-14
Start date
2022-09-08
Completion date
Unknown
Last updated
2025-05-19

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

Conditions

Myopia

Interventions

Experimental group:Wear a peripheral defocusing lens
Control group:Wear a regular single focus lens

Sponsors

Xiamen University Xiamen Eye Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 13 Years

Inclusion criteria

Inclusion criteria: Patients must meet the following selection criteria during screening and visits: 1. 6 <= Age<13 years old, gender not limited 2. The refractive status meets the following conditions: 1) After ciliary muscle paralysis, the computer optometry test showed that the equivalent spherical photometry of both eyes was between -0.5D and -4.0D (including -0.50D and -4.0D), 2) Computer optometry detection of astigmatism in both eyes after ciliary muscle paralysis <= 1.50D 3) Computer optometry detection of anisometropia <= 1.5D in both eyes after ciliary muscle paralysis 3. Parents/guardians understand the case and are willing to accept random grouping

Exclusion criteria

Exclusion criteria: Patients who meet any of the following criteria during screening and random visits are not eligible to participate in this study 1. Either eye has refractive system abnormalities such as macula/opacities, cone-shaped opacities, lens opacities, uveitis, macula abnormalities, retinal lesions, etc 2. Either eye has a history of glaucoma 3. Obvious strabismus, amblyopia, or previous refractive surgery 4. Previous or current use of atropine, OK lens, defocusing lens, hard film contact lens 5. Previous systemic diseases: immune system diseases, central nervous system diseases, asthma, diabetes, lung dysfunction, liver and kidney dysfunction 6. Take belladonna, morphine, sleeping pills, etc 7. Have a clear family history of high myopia 8. Researchers believe that there are any other circumstances that are not suitable for participating in the experiment

Design outcomes

Primary

MeasureTime frame
Equivalent spherical photometry;

Secondary

MeasureTime frame
Optic axis;Percentage of equivalent spherical photometry progress<-0.50D;Percentage of equivalent spherical photometry progress<-0.75D;Percentage of equivalent spherical photometry progress<-1.00D;

Countries

China

Contacts

Public ContactXiaoxin Li

Xiamen University Xiamen Eye Center

drlixiaoxin@163.com+86 138 0115 3661

Outcome results

None listed

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