ACTRN12618000242224终止未知
Prospective, contralateral, randomised, crossover dispensing clinical trialto compare the myopia progression rate between a myopia control contactlens and single vision contact lenses
Brien Holden Vision Institute0 个研究点目标入组 10 人开始时间: 2018年2月14日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 终止
- 发起方
- 入组人数
- 10
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 6 Years 至 17 Years(—)
- 性别
- All
入选标准
- •Aged between 6 years to 17 years (6 years and 17 years inclusive);
- •Spherical equivalent -0.75 D to -3.50 D with cylinder no more than -1.00 D; anisometropia of less than or equal to 0.75D
- •Able to read and comprehend English and give informed consent as demonstrated by signing a record of informed consent or have a parent / guardian who is able to give informed consent on the participant’s behalf.
- •Be willing to comply with the wearing and clinical trial visit schedule as directed by the investigator;
- •Have ocular health findings considered to be normal” and which would not prevent the subject from safely wearing contact lenses;
- •Have vision correctable to at least 6/9.5 or better in each eye with study contact lenses.
排除标准
- •Participants enrolled in the trial must NOT have:
- •pre-existing ocular irritation that would preclude contact lens fitting;
- •any systemic or ocular condition or ocular injury that may preclude safe wearing of contact lenses;
- •undergone corneal refractive surgery;
- •Keratoconus
- •a known allergy to, or a history of intolerance to cyclopentolate or topical anaesthetics;
- •at baseline, astigmatism more than 1.00 D in either eye;
- •had strabismus and/or current ongoing amblyopia;
- •any ocular, systemic or other condition or disease with possible associations with myopia or affecting refractive development e.g. Marfan syndrome, retinopathy of prematurity;
- •current orthoptic treatment or vision training;
- •eye injury or surgery within 12 weeks immediately prior to enrolment for this trial;
- •undergone atropine treatment for myopia control;
- •worn bifocal or progressive addition spectacles or anti-myopia contact lenses previously;
- •worn orthokeratology lenses previously;
- •require anticholinergic medication for gastrointestinal or other conditions;
- •at baseline, be anisometropic by more than 0.75D;
研究者
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