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Sustained and rebound effects of Low-intensity red-light therapy on myopia control: a 2-year follow-up study

Sustained and rebound effects of Low-intensity red-light therapy on myopia control: a 2-year follow-up study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400079987
Enrollment
Unknown
Registered
2024-01-17
Start date
2024-02-01
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

myopia

Interventions

SVS-LLLT:Wear myopic frame glasses (optical monocal lens) turn to Low-intensity red-light therapy groups
LLLT-SVS:Low-intensity red-light therapy groups turn to Wear myopic frame glasses (optical monocal lens)

Sponsors

Eye Hospital of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
9 Years to 13 Years

Inclusion criteria

Inclusion criteria: 1. A Study on the safety and effectiveness of myopia and amblyopia comprehensive therapeutic instrument for controlling myopia progression in children and adolescents that has been previously enrolled and completed. 2. Sign the informed consent form. 3. Patient is capable and willing to follow the study protocol as judged by the investigator.

Exclusion criteria

Exclusion criteria: 1.Have used any myopia control methods within 3 months, such as medications, peripheral defocus frames, and contact lenses (except for the experimental group that has been treated with Low-intensity red-light therapy for one year); 2. Any eye diseases (such as cataracts, congenital retinal diseases, amblyopia, and strabismus); 3. Children with refractive media opacity or refractive media intervention related surgeries, such as cataract surgery, corneal transplantation, corneal leukoplakia, keratoconus, etc.; 4. Presence of systemic diseases that may affect refractive status, such as Marfan syndrome, Macessanne syndrome, type 1 diabetes mellitus, etc.; 5. Shallow anterior chamber, glaucoma, and family history of glaucoma; 6. Children who cannot cooperate with the examination, children who withdraw in the middle of the inspection.

Design outcomes

Primary

MeasureTime frame
Axial length;

Secondary

MeasureTime frame
Spherical equivalent;Choroidal thickness;

Countries

China

Contacts

Public ContactChen Jie

Eye Hospital of Wenzhou Medical University

cj@eye.ac.cn+86 138 5772 1998

Outcome results

None listed

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