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临床试验/NCT06016231
NCT06016231已完成不适用

Clinial Outcomes of Bilateral Pseudophakic Patients with a Light Adjustable Lens (LAL) Implanted in At Least One Eye

Bucci Laser Vision Institute1 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2023年8月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
24
试验地点
1
主要终点
Patient Satisfaction - subjective questionnaire

研究概览

简要总结

To collect data on bilateral pseudophakic patients implanted with the RxSight Light Adjustable Lens (LAL) in at least one eye

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Cross Sectional

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adults with bilateral pseudophakia who have been implanted with the LAL in at least one eye and who have completed LDD light treatments

排除标准

  • Visually significant eye disease

结局指标

主要结局

Patient Satisfaction - subjective questionnaire

时间窗: 3-18 months after cataract surgery

Subjective questionnaire explores the frequency/need for glasses for various visual functions at distance/intermediate/near, experience with dysphotopsias, and overall satisfaction of visual function without glasses.

次要结局

未报告次要终点

研究者

发起方
Bucci Laser Vision Institute
申办方类型
Other
责任方
Sponsor

研究点 (1)

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