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临床试验/JPRN-jRCT1032200350
JPRN-jRCT1032200350招募中未知

Wear Study of Daily Disposable Silicone Hydrogel Lensclariti 1 day

kodama yuji0 个研究点目标入组 60 人开始时间: 2021年2月5日最近更新:

试验速览

阶段
未知
状态
招募中
发起方
入组人数
60

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 18age old 至 ot applicable(—)
性别
All

入选标准

  • 1.Subjects aged 18 years or older at the time of informed consent. However, if the subject is a minor (younger than 20 years), written informed consent should be obtained from his/her parent (legal representative).
  • 2.Subjects who understand the purpose of this study and sign the informed consent form to participate in this study
  • 3.Subjects who wear SCLs every day and agree to use the study lens as a 1-day disposable lens
  • 4.Subjects to whom the study lens can be prescribed within its power range
  • 5.Subjects who can comply with the method of use and visit the medical institution in accordance with the specified schedule
  • 6.Subjects who wear daily disposable hydrogel SCLs other than the products marketed by the sponsor in Japan
  • 7.Subjects who have no abnormal findings that would be problematic for CL wearing in the anterior eye

排除标准

  • 1.Subjects who plan to wear the lens for monocular vision or use the lens only for 1 eye
  • 2.Subjects with aphakia or eyes implanted with artificial intraocular lenses
  • 3.Subjects with systemic disease that may affect the eyes
  • 4.Subjects who are using drugs that may affect the visual function and performance of the study lens
  • 5.Subjects with corneal infiltration or corneal ulcer
  • 6.Subjects who have undergone corneal surgery (refractive surgery, etc.)
  • 7.Subjects who are participating in other clinical studies or researches
  • 8.Other subjects who are judged to be inappropriate by the investigator

研究者

发起方
kodama yuji

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Wear Study of clariti 1 day | 临床试验