跳至主要内容
临床试验/NCT00938951
NCT00938951已完成不适用

Evaluate the Ability of Systane Ultra to Improve Subjective Symptoms of Ocular Irritation Post 60 Min. Athletic Performance.

Alcon Research0 个研究点目标入组 16 人开始时间: 2009年6月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
16
主要终点
Effectiveness of eye drop basd on athlete's opinion/experience during a one hour practice session

研究概览

简要总结

The primary objective of this study is to compare visual degradation in a stressed (forced stare) environment in patients before and after acute administration of Systane Ultra.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Supportive Care
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
是

入选标准

  • •Player/ Coach must answer "Yes" to the survey eligibility question.
  • •Player/Coach must voluntarily agree to participate in survey

排除标准

  • 未提供

研究组 & 干预措施

Systane® Ultra

Experimental

Systane® Ultra

干预措施: Systane® Ultra (Other)

结局指标

主要结局

Effectiveness of eye drop basd on athlete's opinion/experience during a one hour practice session

时间窗: 60 minutes post-dosing with test article

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

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