DRKS00012740已完成不适用
Post-Market Clinical Follow-Up Study Evaluating Safety and Performance of HOYA IOLs in Routine Practice - PMCF-101-LONG
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 784
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 22 Years 至 one（—）
- 性别
- All
入选标准
- •1. Minimum 22 years of age
- •2. Planned natural lens replacement with posterior chamber IOL implantation
- •3. Available and comply to study procedures
- •4. Ability and willingness to sign informed consent
排除标准
- •1. Participation in this PMCF with the other eye.
- •2. Patient is pregnant, plans to become pregnant, is lactating or has another condition associated with the fluctuation of hormones that could lead to refractive changes
- •3. Concurrent participation or participation within 30 days prior to preoperative visit in any other clinical trial with an investigational product
研究者
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