Fundus Effects of Repeated Low-Level Red-Light Therapy in Chinese Myopic Minors: A Randomized Controlled Clinical Trial
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 70
- 试验地点
- 1
- 主要终点
- Latency of P1 waves
研究概览
简要总结
- Research Objective: The primary objective is to investigate the short-term effects of repetitive low-intensity red light therapy on the fundus of the eyes of underage individuals with myopia.
- Research Design: This experiment employs a prospective, single-center, randomized, controlled clinical research design.
- Primary Outcome: Changes in macular sensitivity (microperimetry).
- Recruitment and Participant Information: The study population consists of individuals aged 7 to 17 years old. It is anticipated that there will be 35 participants in both the control group and the experimental group.
- Trial Location: Zhongshan Ophthalmic Center, Sun Yat-sen University. Contact Information: Shuyu Chen, +190805155537, chenshuyu980916@163.com.
详细描述
- Research Design: This study is an interventional research aimed at investigating the short-term effects of repeated low-intensity red light therapy on the fundus of underage individuals with myopia. Retinal light damage typically occurs in the photoreceptor layer and retinal pigment epithelium. Optical coherence tomography angiography (OCTA), OCT, pattern visual evoked potentials (VEP), microperimetry, and multifocal electroretinography (ERG) will be utilized to assess the functionality of the retina, choroid, and optic nerve, thus identifying potential areas of damage. This will provide a scientific basis for further evaluating the safety of low-intensity red light therapy.
- Participant Recruitment:
(1) Age range: 7 to 17 years old. (2) Spherical equivalent refraction (SER): -1.00D to -5.00D. (3) Astigmatism: ≤ 2.50D. (4) Anisometropia (difference between the two equivalent spherical lenses): ≤ 1.50D.
(5) Best corrected visual acuity (BCVA) in either eye: ≥ 20/20. (6) Willingness to undergo low-intensity red light treatment. (7) Ability to comprehend the trial's purpose, voluntary participation, and signing of an informed consent form by the subject and their legal guardian.
3.Intervention:Control Group: Daily wear of frame glasses for refractive correction, without any additional treatment for myopia control.Experimental Group: Daily wear of frame glasses for refractive correction, along with low-intensity red light therapy as prescribed by the optometrist.
4.Data Collection: All examinations are conducted by experienced doctors，technicians, and optometrists during objective assessments. Data collection forms are incorporated into the medical records. Specialized research coordinators conduct regular follow-up with all subjects via telephone or WeChat.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Other
- 盲法
- Double (Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 7 Years 至 17 Years（Child）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •7~17 years old；
- •Spherical equivalent refraction (SER) -1.00 to -5.00D；
- •Astigmatism≤ 2.50D；
- •Anisometropia (difference between the two equivalent spherical lenses) ≤ 1.50D；
- •Best corrected visual acuity (BCVA) in either eye ≥ 20/20；
- •Currently willing to use low-intensity red light treatment；
- •Be able to understand the purpose of the trial, voluntarily participate and have the subject and his legal guardian sign an informed consent form.
排除标准
- •strabismus (apparent strabismus) or amblyopia；
- •Correction of abnormal vision in either eye；
- •Any eye disease that may be related to myopia or affect refractive development, such as history of photosensitivity, macular disease, moderate to severe dry eye, corneal disease, cataract, vitreoretinal disease, infectious conjunctivitis, uveitis, optic nerve damage, congenital optic nerve development abnormalities or other eye diseases；
- •Systemic diseases, such as hypertension, lupus erythematosus, albinism, diabetes, etc；
- •previous history of convulsions, tics, central nervous system underdevelopment, psoriasis, epilepsy and psychiatric and psychological diseases；
- •used within 3 months or planned to use low-concentration atropine eye drops during the study；
- •Those who have previously used orthokeratology lenses, peripheral defocusing glasses, multifocal soft lenses and other optical therapies to control the progression of myopia, and the elution period is less than three months；
- •Other situations in which the investigator believes that the patient is not suitable to participate in this study.
结局指标
主要结局
Latency of P1 waves
时间窗: Immediately、1 day、1 month、3 months、6 months after treatment
Multifocal electroretinogram (mfERG) was used to detect the electrophysiological activity of the local retina of the macula, and the latency of P1 wave was recorded.
次要结局
- Amplitude and latency of P100 waves(Immediately、1 day、1 month、3 months、6 months after treatment)
- Choroidal thickness(Immediately、1 day、1 month、3 months、6 months after treatment)
- Amplitude of P1 waves(Immediately、1 day、1 month、3 months、6 months after treatment)
- Choroidal and retinal blood flow density assessment(Immediately、1 day、1 month、3 months、6 months after treatment)
- Changes in visual acuity in the macula (microperimetry)(Immediately、1 day、1 month、3 months、6 months after treatment)
研究者
Jin Ma
Professor at Sun Yat-sen University, Chief Physician at Sun Yat-sen University Hospital, and Doctoral Supervisor at Sun Yat-sen University.
Zhongshan Ophthalmic Center, Sun Yat-sen University