DRKS00020388已完成未知
Postmarket Study of outcomes from WaveLight® EX500 InnovEyes™ treatment in conjunction with the InnovEyes™ Sightmap - RFP911-P001
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 136
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- N/a: Single Arm Study
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 21 Years 至 one（—）
- 性别
- All
入选标准
- •Minimum of 21 years of age
- •- Myopia up to and including -11.00 D with or without astigmatism up to -4.50 D
- •- BCDVA of 20/20 or better
- •Other protocol-defined inclusion criteria may apply
排除标准
- •- Acute or chronic disease or illness that would increase the operative risk or confound the outcomes of the study.
- •- Previous intraocular or corneal surgery
- •- Participation in other clinical trials during the course of the study that may
- •confound study results
- •Other protocol-defined exclusion criteria may apply.
研究者
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