NCT01731743已完成不适用
Evaluation of Visual Acuity and Patient Satisfaction With AT LISA TRI 839MP Intraocular Lenses
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 107
- 试验地点
- 2
- 主要终点
- Intermediate visual acuity
研究概览
简要总结
The purpose of the study is to evaluate the far, intermediate and near visual acuities with a trifocal IOL.
详细描述
After bilateral cataract surgery, monocular and binocular uncorrected (UCVA) and best distance corrected visual acuity (BCVA) will be measured at far (4m), intermediate (80 cm) and near (40 cm) distance as well as the subjective refraction.
A patient questionnaire will be used to assess the patient satisfaction and spectacle independence.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 50 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Man or woman, over 50 years of age
- •Bilateral implantation of a trifocal intraocular lens
- •Capsular bag implantation
排除标准
- •Existing ocular pathology
- •Surgical complications
- •Corneal astigmatism ≥ 1.0D
研究组 & 干预措施
implantation of a trifocal IOL (AT LISA tri 839MP)
Other
干预措施: AT LISA tri 839MP (Device)
结局指标
主要结局
Intermediate visual acuity
时间窗: up to 3 months postoperatively
Monocular and binocular uncorrected and best distance corrected
次要结局
- near and far visual acuity(1 and 3 month postoperatively)
研究者
研究点 (2)
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