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Safety and Efficacy Evaluation of Different Types of Repeated Low-Level Red-Light Therapy for Myopia Control in Children

Safety and Efficacy Evaluation of Different Types of Repeated Low-Level Red-Light Therapy for Myopia Control in Children

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500115347
Enrollment
Unknown
Registered
2025-12-25
Start date
2025-12-25
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Myopia

Interventions

650nm Diffuse RLRL group:650nm Diffuse RLRL
650nm RLRL group:650nm laser RLRL
650nm LED RLRL group:650nm LED RLRL group

Sponsors

Tianjin Medical University Eye Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
8 Years to 13 Years

Inclusion criteria

Inclusion criteria: 1: 8–13 year old , regardless of gender 2: Spherical Equivalent Refraction (SER) -4.00 D to -0.50 D 3: Astigmatism <2.50 D 4: Anisometropia<1.50 D 5: No other organic ocular diseases affecting vision in both eyes 6: The subject and their guardian are able to understand the purpose of this trial, sign the informed consent form, and the subject can cooperate with the treatment and related ophthalmic examinations. No other myopia control measures apart from the study protocol will be adopted during the entire research period

Exclusion criteria

Exclusion criteria: 1: Previous myopia control treatments such as anticholinergic drugs (e.g., atropine) within the past 3 months, or participation in other functional spectacle lenses, functional soft contact lenses, etc. 2: Diagnosed color vision abnormalities 3: History of photosensitivity, glaucoma, glaucomatocyclitic crisis, ocular hypertension, macular lesions, or retinal damag 4: Systemic diseases involving the heart, liver, kidneys, etc., or congenital hereditary myopia 5: Ocular trauma, manifest strabismus, history of eye surgery, chronic eye conditions such as allergic conjunctivitis, etc 6: Pre-existing conditions such as entropion or trichiasis, severe corneal or conjunctival infections, or other ocular diseases 7: Neurological disorders, allergies or contraindications to atropine or other therapeutic drugs 8: Patients with systemic or autoimmune diseases such as albinism, psoriasis, nephrotic syndrome, systemic lupus erythematosus, diabetes, etc. 9: Any other conditions deemed by the researcher as unsuitable for participation in the study

Design outcomes

Primary

MeasureTime frame
Changes of axial length;

Secondary

MeasureTime frame
Changes in Spherical Equivalent;Changes in Choroidal Thickness;Changes of axial length, Spherical Equivalent, Choroidal Thicknessafter withdrawal;

Countries

China

Contacts

Public ContactYang Jing

Tianjin Medical University Eye Hospital

hiyangjing101246@hotmail.com+86 86428756

Outcome results

None listed

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