NCT01214863已完成不适用
Clinical Results With the AcrySof Toric Intraocular Lens (IOL)
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 144
- 试验地点
- 1
- 主要终点
- Visual Acuity
研究概览
简要总结
This study is an evaluation of visual outcomes of subjects implanted with the AcrySof Toric Intraocular Lenses (IOLs) Models SN60T3, SN60T4, and SN60T5.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Only
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Diagnosed with cataracts; has astigmatism falling in range of AcrySof Toric lens as assessed by the AcrySof Toric calculator
排除标准
- •Ocular comorbidities affecting visual outcome data,
- •Prior refractive surgery,
- •Irregular astigmatism
结局指标
主要结局
Visual Acuity
时间窗: 1 day to 6 months
次要结局
- Postoperative refractive cylinder(1day to 6 months)
研究者
研究点 (1)
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