A Single-Center, Cross-over, Pilot Study Evaluating Acuvue® Oasys® Lenses (Senofilcon A), 30-Day Bausch + Lomb PureVision (Balafilcon A), and Clariti® 1-Day (Somofilcon A) Lenses, for Their Impact on Ocular Discomfort Induced by Exposure to the Turbo Controlled Adverse Environment™
试验速览
- 阶段
- 不适用
- 状态
- 撤回
- 发起方
- 试验地点
- 1
- 主要终点
- Contact lens wear comfort, as assessed by subject reported symptoms in diaries.
研究概览
简要总结
The purpose of this study is to compare the comfort of three commercially available contact lenses.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Treatment
- 盲法
- Double (Participant, Investigator)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Be at least 18 years old
- •Have provided written informed consent
- •Have discomfort when wearing contact lenses
排除标准
- •Have an active ocular infection or significant slit lamp findings
- •Participated in any other studies in the past 30 days
研究组 & 干预措施
Clariti® 1-Day (Somofilcon A)
Clariti® 1-Day (Somofilcon A) contact lenses
干预措施: 30-Day Bausch + Lomb PureVision (balafilcon A) (Device)
Acuvue®Oasys® Lenses(senofilcon A)
Acuvue® Oasys® Lenses (senofilcon A) contact lenses
干预措施: Acuvue® Oasys® Lenses (senofilcon A) (Device)
Acuvue®Oasys® Lenses(senofilcon A)
Acuvue® Oasys® Lenses (senofilcon A) contact lenses
干预措施: 30-Day Bausch + Lomb PureVision (balafilcon A) (Device)
Acuvue®Oasys® Lenses(senofilcon A)
Acuvue® Oasys® Lenses (senofilcon A) contact lenses
干预措施: Clariti® 1-Day (Somofilcon A) (Device)
Bausch + Lomb PureVision (balafilcon A)
30-Day Bausch + Lomb PureVision (balafilcon A) contact lenses
干预措施: Acuvue® Oasys® Lenses (senofilcon A) (Device)
Bausch + Lomb PureVision (balafilcon A)
30-Day Bausch + Lomb PureVision (balafilcon A) contact lenses
干预措施: 30-Day Bausch + Lomb PureVision (balafilcon A) (Device)
Bausch + Lomb PureVision (balafilcon A)
30-Day Bausch + Lomb PureVision (balafilcon A) contact lenses
干预措施: Clariti® 1-Day (Somofilcon A) (Device)
Clariti® 1-Day (Somofilcon A)
Clariti® 1-Day (Somofilcon A) contact lenses
干预措施: Acuvue® Oasys® Lenses (senofilcon A) (Device)
Clariti® 1-Day (Somofilcon A)
Clariti® 1-Day (Somofilcon A) contact lenses
干预措施: Clariti® 1-Day (Somofilcon A) (Device)
结局指标
主要结局
Contact lens wear comfort, as assessed by subject reported symptoms in diaries.
时间窗: 1 week
次要结局
未报告次要终点