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临床试验/NCT00346593
NCT00346593已完成不适用

Investigation of the Clinical Performance of Silicone Hydrogel Contact Lenses During Continuous Wear

University of Melbourne1 个研究点 分布在 1 个国家开始时间: 2004年5月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
试验地点
1

研究概览

简要总结

The primary purpose of this study is to investigate the clinical performance of a new silicone hydrogel contact lens during continuous wear (up to 30 nights) over a period of 24 months.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Treatment
盲法
Double

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Has had an oculo-visual examination in the last 2 years.
  • •Is correctable to at least 6/7.5 distance visual acuity in each eye with spherical contact lenses.
  • •Is a current soft contact lens wearer.
  • •Has no clinically significant anterior eye findings.
  • •Has no other active ocular disease.

排除标准

  • •Has any systemic disease that might interfere with contact lens wear
  • •Is using any systemic or topical medications that will affect ocular health.
  • •Has any pre-existing ocular irritation that would preclude contact lens fitting.
  • •Has any ocular pathology or severe insufficiency of lacrimal secretion (dry eyes) that would affect the wearing of contact lenses.
  • •Has undergone corneal refractive surgery.
  • •Is pregnant, lactating or planning a pregnancy.

研究者

申办方类型
Other

研究点 (1)

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