Effectiveness of Essilor® Stellest® Lenses in Slowing Down Myopia Progression in Young Adults
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 入组人数
- 42
- 试验地点
- 1
- 主要终点
- Change in axial length (mm)
研究概览
简要总结
It is expected that myopia progression stabilises in the late teenage years, however, some studies report that myopia progression continues through early adulthood in as many as one third of myopes. Similarly, there are reports of myopia commencing in early adulthood. Although the rate of progression is slower than that occurring in childhood, between 20-35% of adults aged between 20-30 years were reported to progress by at least -1.00D over a five year period. Given that every dioptre increase in myopia results in an increased overall lifetime risk of serious ocular pathology, it seems opportune to investigate whether myopia management treatments designed to slow myopia progression in childhood could be beneficial for progressing adult myopes. The proposed study will conduct a prospective, randomised, paired-eye, trial with cross-over to evaluate the efficacy of Essilor Stellest myopia management spectacle lenses on the progression of myopia in adults aged between 18-40 years. The outcomes from the trial will provide novel evidence regarding the utility of these lenses in an adult population.
详细描述
This is a 2-year, prospective, randomised, paired-eye controlled trial with cross-over which will be conducted at Ulster University, Coleraine, Northern Ireland. The trial will evaluate the efficacy of Essilor Stellest myopia management spectacle lenses on the progression of myopia in adults aged between 18-40 years. Participants will act as their own control, wearing a Stellest lens in front of one eye and a single vision lens in front of the fellow eye. At the 12-month visit, lens allocation will be crossed-over between eyes and worn for a further 12 months. Randomisation of whether Stellest will be worn in the dominant or non-dominant eye first will be conducted using permuted block design.
Participants will be asked to wear the study spectacles for at least 12 hours per day, 6 days per week. No other form of myopia management spectacle or contact lens will be worn during the trial period. At the two-year review participants will be given the option of continuing with Stellest lenses in both eyes or reverting to single vision spectacles in both eyes depending on the results of the study. Those participants who continue to wear Stellest lenses (binocularly) will be contacted after one month to investigate the acceptability of Stellest wear in adult myopes.
Participants will be screened at baseline to ensure they meet the inclusion criteria. Participants will be asked if they have ever attended the hospital eye service or have been told they have an eye condition by their optometrists. Fundus images and slit lamp examination will also be conducted at baseline to confirm eye health. Cycloplegic refraction and axial length will be measured at baseline, 6-months and 12-months using the Shin-Nippon NVision-K 5001 and IOLMaster 700 respectively. Cycloplegia will be induced by two drops of 1% tropicamide separated by 5 minutes. Punctal occlusion following instillation of the drop will be applied to reduce systemic absorption.
At 12-months, the crossover will take place. A further assessment of cycloplegic refraction and axial length will be performed 6-months (18-month visit) and 12-months (24-month visit) after the crossover. The following additional measurements will also be made to inform parameters that are associated with better response to treatment and to ensure visual function remains adequate while wearing the study spectacles. These measurements will be taken at baseline and crossover.
- Near and distance visual acuity will be measured using a crowded logMAR letter chart at 33cm and 3m
- Accommodative function will be assessed using dynamic retinoscopy using the UC-Cube
- Binocularity will be assessed using distance and near prism cover test
- Field of vision will be assessed using a Humphrey suprathreshold screening test
- Peripheral refraction will be measured at 30 degrees nasally and temporally
- Choroidal thickness will be measured using a six radial scan using the Heidelberg Spectralis
- Visual comfort will be surveyed by telephone one week after collection of the study spectacles to ensure participants are tolerating the paired-eye control condition
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Treatment
- 盲法
- None
盲法说明
Not possible to mask as participant and/or investigator could identify which lens is 'different' from single-vision through visual inspection.
入排标准
- 年龄范围
- 18 Years 至 40 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Cycloplegic SER less than -0.75D
- •Astigmatism of 1.50D or less
- •Anisometropia of 1.50D or less
- •Evidence of annual progression of myopia of at least 0.50D in the previous two-year period
排除标准
- •Previous myopia management (other than standard spectacle or contact lens correction)
- •Ocular and systemic diseases which might affect visual performance or myopia development
研究组 & 干预措施
A1: Stellest lens wear in front of dominant eye
Stellest lens wear in front of dominant eye.
干预措施: Essilor® Stellest® spectacle lens (Device)
A2: Single vision lens wear in front of non-dominant eye
Single vision lens wear in front of non-dominant eye.
干预措施: Single-vision spectacle lens (Device)
B1: Stellest lens wear in front of non-dominant eye
Single vision lens wear in front of non-dominant eye
干预措施: Essilor® Stellest® spectacle lens (Device)
B2: Single-vision lens wear in front of dominant eye.
Single vision lens wear in front of dominant eye.
干预措施: Single-vision spectacle lens (Device)
结局指标
主要结局
Change in axial length (mm)
时间窗: 2 years
Change in axial length (mm) of the eye wearing the Stellest lens compared to the control eye wearing standard single vision lenses.
Change in cycloplegic autorefraction (D)
时间窗: 2 years
Change in cycloplegic autorefraction (D) of the eye wearing the Stellest lens compared to the control eye wearing standard single vision lenses.
次要结局
- Acceptability to adult patients of Stellest lenses prescribed for both eyes, assessed using the Stellest adult tolerability questionnaire.(1 month)