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临床试验/KCT0009101
KCT0009101尚未招募Unknown

Evaluation of safety and effectiveness of a multimodal imaging device HWSO-1 through comparison of various retinal images:Huvitz HWSO-1 vs Heidelberg Spectralis and Topcon Maestro II(Prospective, single-center, open-label, single-group, post-marketing clinical trial)

Huvitz0 个研究点目标入组 56 人开始时间: 待定最近更新:
适应症

试验速览

阶段
Unknown
状态
尚未招募
发起方
入组人数
56

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
19(Year) 至 80(Year)(—)
性别
All

入选标准

  • 1) Healthy eyes
  • - Adults between the ages of 19 and 80 years old
  • - Those who have given written consent to participate in the study
  • - General healthy eyes: Spherical Equivalent within ±6.00D, corrected visual acuity of 0.25 or better, intraocular pressure of 21mmHg or less, no clinically significant abnormal findings in the anterior segment/ fundus, eye without a surgery(excluding cataracts and refractive surgery) and ocular diseases eyes that will not effect the result under investigator's decision.
  • 2) Ocular disease eyes
  • - Adults between the ages of 19 and 80 years old
  • - Those who have given written consent to participate in the study
  • - subjects who require fundus photography due to eye disease such as retinal disease or glaucoma.

排除标准

  • 1) Pregnant and lactating women
  • 2) Eyes with a media opacity(corneal opacity, severe cataract, vitreous opacity, etc.) that may affect the result by the investigator's decision.
  • 3) Eyes deemed inappropriate by the investigator.

研究者

发起方
Huvitz

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