ISRCTN12292232已完成未知
Randomised trial of a personalised dosing strategy versus a standardised dosing strategy for childhood amblyopia
City University London (UK)0 个研究点目标入组 120 人开始时间: 2013年12月17日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 120
研究概览
简要总结
2015 protocol in: http://www.ncbi.nlm.nih.gov/pubmed/25906974
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. The trial will recruit subjects with amblyopia associated with:
- •1.1. Strabismus
- •1.2. Anisometropia
- •1.3. A combination of anisometropia and strabismus
- •2. Children aged between 3 and 8 years with visual acuity of 0.2 logMAR or lower in the worst eye and an inter-ocular difference of at least 0.2 log units with the presence of anisometropia and/or strabismus and no other ocular pathology including amblyopia associated with form deprivation or previous occlusion treatment history will be eligible for recruitment.
- •3. Target Gender: Male & Female
排除标准
- •1. Those with other ocular pathology
- •2. Those with form deprivation amblyopia as this is a minority group and often is linked with other ocular pathology
- •3. Previous history of treatment for amblyopia
- •4. Those with learning difficulties and therefore cannot perform an accurate visual acuity test on every occasion tested
研究者
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