DRKS00023571已完成4 期
Prospective, single-center PMCF * study to check the IOL constant with recording of vision, contrast vision and patient satisfaction after bilateral implantation of a glistening-free, hydrophobic, multifocal IOL - ACUNEX-Study
Teleon Surgical Van Rensselaerweg 4bNL- 6956 AV Spankeren Teleon Surgical Vertriebs GmbH0 个研究点目标入组 23 人开始时间: 2020年12月11日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 23
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
- 18 Years 至 85 Years（—）
- 性别
- All
入选标准
- •patient age> 30 years
- •- Bilateral cataract / bilateral supply
- •- expected postoperative corneal astigmatism = 1.00 dpt
- •- Planned implantation in the capsular bag
- •- photopic pupil size = 2.8 mm
- •- Pupil decentering <0.8 mm (center shift)
- •- Contact lens break of at least 2 weeks
- •- a written declaration of consent of the patient
排除标准
- •- amblyopia, strabismus
- •- Irregular Corneal Astigmatism Pathology of the cornea and retina
- •- Diseases of the eye which, apart from the cataract, can lead to a reduction in the decimal visual acuity to 0.63 or worse
- •- intraoperative complications
- •- current active participation in another clinical study of the patient
研究者
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