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临床试验/jRCT1032240342
jRCT1032240342招募中不适用

Study of Intraocular Lens Constants for the Intraocular Lens HOYA Vivinex Impress Implanted Eyes

HOYA CORPORATION0 个研究点目标入组 900 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
900
主要终点
-

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
22age old over 至 No limit(—)
性别
All

入选标准

  • Patients who are 22 years old or older and who are undergoing cataract extraction with phacoemulsification and aspiration
  • Patients who are having XY1-EM implanted
  • Patients whose calculated spherical lens power is +6.0 D or higher and +30.0 D or lower
  • Patients whose postoperative corrected visual acuity can be expected to be 0.7 or better
  • Patients whose preoperative corneal astigmatism is below 1.0 D
  • Patients who can be followed-up with after surgery

排除标准

  • Patients who are having another ophthalmologic surgery within one month after the intraocular lens implantation
  • Patients who have a history of refractive surgery
  • Patients who have a history of any eye disease or ocular comorbidities that significantly affect their visual function
  • Patients who the principal investigator, etc., deems not appropriate as a study subject due to an accompanying general disease or eye disease

结局指标

主要结局

-

IOL constant per intraocular lens formula by biometers

次要结局

未报告次要终点

研究者

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