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Effectiveness of soft contact lens for myopia control based on the theory of peripheral retinal defocus

Effectiveness of soft contact lens for myopia control based on the theory of peripheral retinal defocus

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000041520
Enrollment
Unknown
Registered
2020-12-27
Start date
2021-06-05
Completion date
Unknown
Last updated
2026-06-15

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

Conditions

Myopia

Interventions

Group 1:The subjects' eyes were randomly assigned to wear an orthokeratology lens (OK lens) in one eye and a soft contact lens in the fellow eye
after a 4-week washout period, the wearing methods were exchanged for both eyes. The eyes in this group received OK lens intervention in the first year, and the soft lens intervention eyes in the seco
Group 2:The subjects' eyes were randomly assigned to wear an orthokeratology lens (OK lens) in one eye and a soft contact lens in the fellow eye
after a 4-week washout period, the wearing methods were exchanged for both eyes. The eyes in this group received soft lens intervention in the first year, and the OK lens intervention eyes in the seco

Sponsors

Optometry Hospital Affiliated to Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
8 Years to 12 Years

Inclusion criteria

Inclusion criteria: 1. Aged 8–12 years; 2. History of myopia progression greater than –0.50D per year with previous spectacles; 3. Spherical equivalent refraction: –0.75D to –5.00D; astigmatism: <=–1.50D; 4. Anisometropia: <= 1.00D; 5. Normal binocular vision function (including stereopsis); 6. No other organic ocular diseases; 7. No history of rigid contact lens wear, atropine treatment, or multifocal spectacle use.

Exclusion criteria

Exclusion criteria: 1. Those with a history of ocular trauma or surgery; 2. Patients with dry eye syndrome; 3. Previous use of medications related to myopia control (e.g., atropine eye drops); 4. Those with poor cooperation or who have acquired images of insufficient quality.

Design outcomes

Primary

MeasureTime frame
Two-year change in axial length;Two-year change in spherical equivalent;

Secondary

MeasureTime frame
Change in choroidal thickness;Rate of change in retinal blood flow density;Changes in corneal biomechanical parameters (measured by Corvis ST);meibomian gland scores;Non-invasive Keratograph Break-up (NIKBUT);Tear Meniscus Height(TMH);

Countries

China

Contacts

Public ContactYunjie Zhang

Optometry Hospital Affiliated to Wenzhou Medical University

zhang_yj530@163.com+86 137 5082 8781

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 21, 2026