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Study on the control of myopia with circular column lens modulation

Study on the control of myopia with circular column lens modulation

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100053711
Enrollment
Unknown
Registered
2021-11-28
Start date
2020-08-01
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Myopia

Interventions

Control group:One point frame glasses
Experimental group:Circular cylindrical mirror modulation lens

Sponsors

Affiliated Eye Hospital of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
8 Years to 12 Years

Inclusion criteria

Inclusion criteria: 1. Aged 8 to 12 years; 2. Binocular myopia -1.0D~-4.0DS, astigmatism <=1.5DC, and binocular myopia difference <=1.0D; 3. The best corrected visual acuity is greater than or equal to 1.0; 4. Birth weight greater than 1500g; 5. Subjects and their legal guardians must sign an informed consent form, be willing to cooperate with treatment and follow-up, and voluntarily participate in this study.

Exclusion criteria

Exclusion criteria: 1. Squint; 2. Amblyopia; 3. Wearing contact lenses or using other programs for myopia treatment (refractive surgery, progressive multifocal lenses, orthokeratology lenses, etc.) within the first six months of enrollment; 4. Eye surgery, trauma or other chronic eye diseases; 5. Systemic diseases, such as respiratory system diseases, cardiovascular system diseases, etc.

Design outcomes

Primary

MeasureTime frame
Ocular axial length;

Secondary

MeasureTime frame
diopter;Choroid thickness;Choroidal blood flow;Retinal thickness;Retinal blood flow;

Countries

China

Contacts

Public ContactMaoXinjie

Affiliated Eye Hospital of Wenzhou Medical University

mxj@mail.eye.ac.cn+86 13705880472

Outcome results

None listed

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