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Myopia control efficacy of peripheral defocus spectacle lenses, Orthokeratology and low dose atropine.

Myopia control efficacy of peripheral defocus spectacle lenses, Orthokeratology and low dose atropine.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500107008
Enrollment
Unknown
Registered
2025-08-01
Start date
2025-08-01
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

PDSLpm:Peripheral defocus spectacle lenses(DIMS or HALT)
ATP:0.01% atropine eye drops
Myopic eye defocus frame lens group:Peripheral defocus spectacle lenses(DIMS or HALT)
OK:OK lens(Alpha or iBright)
Myopia combination treatment group:Combined peripheral defocus spectacle lenses and 0.01% atropine eye drops

Sponsors

Zhujiang Hospital of Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Diagnosed refractive error (myopia or pre-myopia), astigmatism = 0.8; 2.During the observation period, same intervention was consistently used for >= 12 months; 3.baseline and 12-month-follow up data were completed.

Exclusion criteria

Exclusion criteria: 1.Presence of ocular diseases such as strabismus (except heterophoria), amblyopia, keratoconus, glaucoma, or fundus disorders (e.g., history of retinal detachment); 2.Concurrent use of other myopia control interventions (e.g., defocus soft contact lenses, red light therapy devices) during or within 3 months prior to the study; 3.Systemic diseases affecting refractive development (e.g., Marfan syndrome, diabetes).

Design outcomes

Primary

MeasureTime frame
Axial length;

Countries

China

Contacts

Public ContactLin Shunchao

Zhujiang Hospital of Southern Medical University

dennislam@hkcmer.com+86 19210486164

Outcome results

None listed

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