跳至主要内容
临床试验/DRKS00034678
DRKS00034678招募中不适用

IOL comparison study with the RALV device - RALV_IOL-Study

ACMIT Gmbh0 个研究点目标入组 30 人开始时间: 2024年7月15日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
30

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
18 Years 至 40 Years(—)
性别
All

入选标准

  • Refraction: Sphere (Sph): between -3 dpt and +3 dpt
  • Refraction: Cylinder (Cyl): <= 1 dpt
  • Visual acuity >= 1 decimal (or <= 0 logMAR)
  • After the medical examination, the subject was found suitable to receive cyclopentolate eye drops.
  • Informed and signed consent to participate in the study

排除标准

  • Diseases that affect visual acuity (glaucoma, cataract, AMD, corneal opacity or other retinal diseases)
  • Irregular astigmatism
  • Previous eye surgery of any kind
  • In women: pregnancy or breastfeeding

研究者

发起方
ACMIT Gmbh

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