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Effect and safety of peripheral defocus spectacle lenses on myopia prevention among premyopic children

Effect and safety of peripheral defocus spectacle lenses on myopia prevention among premyopic children

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082116
Enrollment
Unknown
Registered
2024-03-21
Start date
2024-04-01
Completion date
Unknown
Last updated
2024-03-25

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

Conditions

premyopia

Interventions

Intervention group 1:Wearing composite defocus incorporated multi-point lenses
Intervention group 2:Wearing defocus incorporated multi-point lenses
Control group:Blank control before myopia onset

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 10 Years

Inclusion criteria

Inclusion criteria: 1. Age: 6-10 years 2. -0.50D < spherical equivalent refraction (SER) = +0.75D 3. Anisometropia = 1.00D 4. Astigmatism = 1.00D 5. Having at least 1 parent with an SER in either eye of -3.00D or less 6. Having not participated in other myopia prevention and control studies, or taken other myopia prevention and control measures, including low-concentration atropine drops, peripheral defocus spectacle lenses, orthokeratology, and multifocal soft lenses within 3 months

Exclusion criteria

Exclusion criteria: 1. Accommodative insufficiency 2. Having eye diseases (e.g. cataract, strabismus, amblyopia, etc.), or having other systemic diseases or developmental abnormalities 3. Poor compliance and the researchers believe that it is not suitable to participate in this clinical trial

Design outcomes

Primary

MeasureTime frame
axial length;diopter;

Secondary

MeasureTime frame
crystalline lens parameters;relative peripheral refraction;choroidal parameters;visual function;visual quality questionnaire;

Countries

China

Contacts

Public ContactLongqian Liu

West China Hospital, Sichuan University

bq15651@hotmail.com+86 189 8060 1759

Outcome results

None listed

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