NCT06488066撤回不适用
Clinical Outcomes of Patients Implanted With the RxSight Light Adjustable Lens (LAL)
适应症
试验速览
- 阶段
- 不适用
- 状态
- 撤回
- 试验地点
- 1
- 主要终点
- Manifest refraction
研究概览
简要总结
The objective of this investigator initiated study (IIT-002) is to collect data on commercial patients implanted with the RxSight Light Adjustable Lens (LAL).
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 40 Years 至 80 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Sign a written Informed Consent Document
- •Implanted commercially with the LAL and completed LDD light treatments
排除标准
- •Previous corneal or intraocular surgery other than removal of cataract and implantation of the LAL
结局指标
主要结局
Manifest refraction
时间窗: Pre operatively and immediately post operatively
A qualified ophthalmologist, optometrist, or a trained ophthalmic technician should obtain the refraction, in 0.25D steps, in a calibrated refraction lane. If the subject has a current pair of glasses for distance vision, they can be measured with a lensometer, and these measurements are used as the beginning approximate refraction
次要结局
未报告次要终点
研究者
研究点 (1)
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