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Clinical study on the effectiveness and safety of myopia control soft contact lenses (crossed dot matrix) in slowing the progression of myopia.

Clinical study on the effectiveness and safety of myopia control soft contact lenses (crossed dot matrix) in slowing the progression of myopia.

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500104065
Enrollment
Unknown
Registered
2025-06-10
Start date
2025-06-14
Completion date
Unknown
Last updated
2025-06-16

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

Conditions

Myopia

Interventions

Test group:To wear a soft contact lens with a dot matrix design, daily disposable. Axial length, OQAS, aberrations, WA5500, choroidal thickness, corneal topography, visual acuity, and visual quality p
Control group:To wear a concentric circle defocus soft contact lenses, daily disposable. Axial length, OQAS, aberrations, WA5500, choroidal thickness, corneal topography, visual acuity were monitored.

Sponsors

Qingdao Eye Hospital Affiliated to Shandong First Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 13 Years

Inclusion criteria

Inclusion criteria: 1. Age >= 6 years old and =-5.00 D, astigmatism = 5.0; 4. Voluntarily participate in this clinical trial and sign an informed consent form;

Exclusion criteria

Exclusion criteria: 1. History of intraocular surgery affecting the use of contact lenses; 2. Clinically significant findings from slit lamp examination; 3. Abnormal results from fundus examination; 4. Abnormal intraocular pressure (IOP 21 mmHg); 5. Presence of other ocular diseases, such as uveitis and various inflammations, glaucoma, cataracts, retinal diseases, ocular tumors, ocular trauma, manifest strabismus; as well as any ocular lesions affecting visual function; 6. Patients with systemic diseases causing immunocompromise (such as diabetes, Down syndrome, rheumatoid arthritis, psychiatric disorders, or other conditions deemed unsuitable for wearing spectacle lenses by the researchers); 7. Only one eye meeting the inclusion criteria; 8. Unable to undergo regular eye examinations; 9. Other situations deemed ineligible by the researchers.

Design outcomes

Secondary

MeasureTime frame
WA5500 Computer Vision Testing;Choroid;Corneal Topography;

Primary

MeasureTime frame
Refractive errors;Axial length;Visual quality parameter;choroid;Periretinal diopter;Accommodation;Aberration;

Countries

China

Contacts

Public ContactXianli Du

Qingdao Eye Hospital Affiliated to Shandong First Medical University

lilibestever@126.com+86 151 9255 2255

Outcome results

None listed

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