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临床试验/NCT05096156
NCT05096156已完成不适用

Evaluation of Wear Experience With PRECISION1® Contact Lenses in Biofinity® Contact Lens Wearers

Ohio State University2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2021年5月28日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
30
试验地点
2
主要终点
Subjective Assessment of Precision1® Daily Disposable Contact Lens

研究概览

简要总结

To evaluate the wear experience of current monthly replacement contact lens wearers after they have been fit into a daily disposable contact lens.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Currently wear Biofinity® monthly replacement spherical contact lenses.
  • Distance visual acuity of 20/25 or better with current contact lenses.
  • Good general health (defined by medication use that has not changed within the last month and the absence of medical conditions or treatments that are deemed confounding to the data as determined by the PI).
  • Ability to give informed consent.
  • Willing to spend time for the study, which includes attending two study visits and wearing contact lenses on days between study visits.

排除标准

  • No current ocular inflammation or infection.
  • Not currently pregnant or lactating.

结局指标

主要结局

Subjective Assessment of Precision1® Daily Disposable Contact Lens

时间窗: 2 weeks

Contact Lens Dry Eye Questionnaire (CLDEQ) survey (0-37, with higher scores related to higher symptoms)

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Jennifer Fogt

PI

Ohio State University

研究点 (2)

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