跳至主要内容
临床试验/NCT04295707
NCT04295707Unknown不适用

Accrued Effect of Orthokeratology for Myopia Control in Children and the Effectiveness of Myopia Control Using an Innovative Orthokeratology Modality. Experiment 1. Effect in Existing Ortho-k Wearers

The Hong Kong Polytechnic University1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2020年3月11日最近更新:
适应症

试验速览

阶段
不适用
入组人数
80
试验地点
1
主要终点
Axial elongation in 2 years

研究概览

简要总结

The two-year prospective study aims at investigating the benefits of frequent replacement (monthly) orthokeratology lenses in myopia control in terms of effectiveness in control and prevention of ocular complications. The secondary objective will be investigating the use of weekly protein removal system in monthly replacement modality orthokeratology lenses on surface deposit.

详细描述

This is a two-year randomized trial. Existing orthokeratology lens wearers (aged 8-13 years), who have completed a 2-year myopia control using orthokeratology, will be recruited and monitored for another two years. Eligible subjects will be randomly assigned to monthly or yearly replacement modality. Axial elongation and ocular conditions will be compared between the monthly and yearly replacement groups.

Subjects on monthly replacement lenses will be randomly assigned to normal cleaning and intensive cleaning groups. Subjects in normal cleaning group will be provided with complimentary contact lenses solutions for daily cleaning and disinfection. In addition to the daily procedures for lens case, subjects in the intensive cleaning group will be required to perform weekly protein removal. All subjects on yearly replacement lenses will be required to performed intensive cleaning such that they will follow normal daily cleaning and disinfection as well as weekly protein removal.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

盲法说明

The outcome assessor was responsible for measuring the axial length and was unaware of the replacement modality of intervention used by the subjects. Another independent examiner will be responsible for grading surface coating from the images taken without disclosure of the information on the cleaning procedures.

入排标准

年龄范围
8 Years 至 15 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Aged 8-15 years
  • Have completed a two-year myopia control study using ortho-k
  • Normal ocular and general condition and not on medication which may contraindicate ortho-k lens wear
  • Pre-ortho-k refractive sphere between -0.75 to -4.00 DS, refractive cylinder ≤ -1.50 DC and anisometropia ≤ -1.00 D
  • Best correctable vision better than 0.08 logMAR in the worse eye
  • Normal binocular function and accommodative status

排除标准

  • Strabismus at distance or near
  • Contraindication for ortho-k lens wear
  • Prior history of ocular surgery, trauma, or chronic ocular disease
  • Systemic or ocular conditions that may interfere refractive development
  • Systemic or ocular conditions that may interfere tear quality and contact lens wear
  • Poor response to the use of study lenses
  • Poor compliance to test procedures
  • Poor compliance to the use of ortho-k lenses (e.g. use of solution, use of lenses)
  • Poor compliance to follow-up schedule

结局指标

主要结局

Axial elongation in 2 years

时间窗: 2 years

Cycloplegic examination of the eyeball length using IOLMaster every 6 monthly

Back Surface Lens Deposits

时间窗: Every month up to 12 months

Surface deposits will be graded using a 4-point scale: 0=no deposit; 1=mild; 2=moderate; 3=severe

次要结局

  • Number of participants with serious adverse effects in 2 years(2 years)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Pauline Cho

Professor

The Hong Kong Polytechnic University

研究点 (1)

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