Efficacy of Multi-Type Photolithography Flat Microstructure Lenses for Childhood Myopia Control

N/ANot Yet RecruitingNCT07535658

Shanghai Eye Disease Prevention and Treatment Center255 enrolled

Overview

The goal of this clinical trial is to learn if photolithographic flat microstructure lenses work to prevent myopia in children. It will also learn about the safety of different designs of photolithographic flat microstructure lenses. The main questions it aims to answer are: Are photolithography flat microstructure lenses effective and safe in preventing myopia in children? Does the depth of tinted lenses affect visual quality? Researchers will compare photolithography flat microstructure lenses to a spectacle lenses with aspherical lenslets to see if photolithography flat microstructure lenses works to prevent myopia in children. Participants will: Wear photolithography flat microstructure lenses or Spectacle Lenses with Aspherical Lenslets more than 8H per day for 1 year. Visit the clinic once every 3 months for checkups and tests.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

PREVENTION

Masking

SINGLE

Enrollment

255

Conditions

Myopia

Interventions

wearing Photolithography Plano Microstructure Lenses incorporates a multi-point defocus optical architecture , featuring photochromic properties with a light transmittance of 55% post-activationDEVICE

Wearing Photolithography Plano Microstructure Lenses incorporates a multi-point defocus optical architecture manufactured by Nuo Tong, featuring photochromic properties with a light transmittance of 55% post-activation for more than 8 hours.

wearing Photolithography Plano Microstructure Lenses designed to reduce contrast sensitivity and featuring a non-fading optical propertyDEVICE

wearing Photolithography Plano Microstructure Lenses designed by Nuo Tong to reduce contrast sensitivity and featuring a non-fading optical property for more than 8 hours

Eligibility

Sex: ALLMin age: 6 YearsMax age: 8 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1. Age: 6 years ≤ age ≤ 8 years (calculated based on the informed consent date); 2. The spherical equivalent (SE) of both eyes is 0D to +1.00D (inclusive of boundary values) after cycloplegia; 3. Astigmatism: Cylindrical power of both eyes ≤ 1.00D; 4. Anisometropia: Difference in spherical equivalent between both eyes ≤ 1.00D; 5. Corrected visual acuity: Best corrected visual acuity (BCVA) of both eyes ≥ 1.0 (decimal notation, 5m); 6. General health status: No systemic syndromes that affect ocular development; no long-term use of growth hormone, corticosteroids, or antiepileptic drugs; 7. Previous intervention: No use of any myopia control methods within the past 3 months, including but not limited to: multifocal glasses, atropine eye drops, red light therapy, acupuncture, etc. 8. Compliance with spectacle wear: Parents ensure that the child wears glasses for ≥8 hours per day; 9. Follow-up capability: Ability to attend scheduled follow-ups for 12 months (4 visits in total); 10. Informed consent from guardian: Legal guardian signs the informed consent form; children also sign the assent form. Exclusion Criteria: 1. History or presence of glaucoma, corneal disease, or other ocular organic disease, or acute or chronic ocular inflammation; 2. Combined with systemic major diseases, mental diseases, or systemic collagen metabolism diseases; 3. Used any myopia intervention drugs or devices in the past 3 months; 4. Those who have participated in other similar clinical studies in the past 3 months; 5. Diagnosis of amblyopia, constant strabismus, and other congenital eye diseases; 6. Those who are allergic to the lens material or products related to the study; 7. Allergy to mydriatic agents and related ophthalmic medications; 8. Allergic to photochromic materials or related dyes; taking photosensitizing drugs; suffering from photo-induced skin or neurological disorders; 9. Unable to understand the study content or unable to cooperate with the follow-up; 10. Other reasons why the research doctor believes the patient is not suitable for the study.

Outcomes

Primary Outcomes

Use 1% cyclopentolate hydrochloride eye drops (Cyclogyl) for cycloplegia and compare the difference in Sphere equivalent refractive changes over 12 months.

Computerized refractometer testing, The formula for calculating sphere equivalent power: sphere power + 0.5 \* cylinder power

Time frame: From enrollment to the end of treatment at 12 month

Secondary Outcomes

Difference in 12-month axial length (AL, mm) from baseline

Measure the length of the eye axis using the IOL Master 700 and compare the difference in eye axis length over 12 months.