DRKS00010108已完成不适用
Observational study to assess clinical outcomes and patient satisfaction after multifocal IOL implantation
Optana GmbH0 个研究点目标入组 28 人开始时间: 2016年3月2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
- 28
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
- 45 Years 至 75 Years（—）
- 性别
- All
入选标准
- •Patients must have read, understood and signed the Patient Information (Informed Consent Form)
- •Patients that underwent uneventful refractive surgery (LASIK, PRK) after cataract surgery can be included
- •Only patients that underwent uneventful cataract surgery with a bilateral implantation of multifocal IO
排除标准
- •Existing posterior capsule opacity (PCO) at the day of study examination
- •The time between the surgeries of both eyes is maximum 3 months
- •Clinically significant glaucoma
- •Clinically significant macular degeneration, clinically significant macular edema or proliferative diabetic retinopathy
- •Patients with keratoconus or keratectasia
- •Patients who are pregnant or nursing
- •Abnormal examination results from slit lamp, fundus examination or IOL Master, topography, age related changes are acceptable
- •Patients who do not give informed consent
研究者
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