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临床试验/NCT04963543
NCT04963543已完成不适用

Evaluation of Comfort in Symptomatic Contact Lens Wearers

Alcon Research2 个研究点 分布在 1 个国家目标入组 17 人开始时间: 2021年7月22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
17
试验地点
2
主要终点
Comfort, collected for each eye

研究概览

简要总结

The purpose of this study is to evaluate the comfort of an ocular lubricant in symptomatic contact lens wearers. This study will be conducted in Canada.

详细描述

The duration of individual participation is six days.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Is able to understand and sign an approved information consent letter;
  • Habitually wears daily disposable soft contact lenses in both eyes;
  • Is able to achieve 20/40 or better monocular VA with habitual contact lenses;
  • Has a pair of spectacles for vision correction.
  • Other protocol-defined inclusion criteria may apply.

排除标准

  • Routinely sleeps in habitual contact lenses;
  • Has any known active ocular disease and/or infection;
  • Is pregnant or lactating;
  • Other protocol-defined exclusion criteria may apply.

结局指标

主要结局

Comfort, collected for each eye

时间窗: Up to Day 6

A visual analogue scale will be used

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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