NCT06758076已完成不适用
A Clinical Comparison of Two Soft Contact Lenses (C24-755)
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
- 52
- 试验地点
- 1
- 主要终点
- Subjective Overall Score
研究概览
简要总结
The aim of this study is to compare the short-term clinical performance of two soft contact lenses.
详细描述
The aim of this study is to evaluate the short-term clinical performance of two soft contact lenses when compared to each other after 15 minutes of daily wear each.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Crossover
- 主要目的
- Treatment
- 盲法
- Single (Participant)
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
- •They are of legal age (18) and capacity to volunteer.
- •They understand their rights as a research subject and are willing and able to sign a Statement of Informed Consent.
- •They are willing and able to follow the protocol.
- •They currently wear soft contact lenses, or have done so within the past two years.
- •They are expected to be able to be fitted with the study lenses within the power range available.
排除标准
- •They have an ocular disorder which would normally contra-indicate contact lens wear.
- •They have a systemic disorder which would normally contra-indicate contact lens wear.
- •They are using any topical medication such as eye drops or ointment.
- •They are aphakic.
- •They have had corneal refractive surgery.
- •They have any corneal distortion resulting from previous hard or rigid lens wear or have keratoconus.
- •They are pregnant or breastfeeding.
- •They have an eye or health condition including an immunosuppressive or infectious disease which would, in the opinion of the investigator, contraindicate contact lens wear or pose a risk to study personnel; or a history of anaphylaxis or severe allergic reaction.
- •They have taken part in any contact lens or care system clinical research within two weeks prior to starting this study.
研究组 & 干预措施
Lens 1 (ocufilcon D)
Experimental
All participants will wear lens 1 for 15 minutes (Period 1).
干预措施: Lens 1 (ocufilcon D) (Device)
Lens 2 (somofilcon A)
Experimental
All participants will wear lens 2 for 15 minutes (Period 2).
干预措施: Lens 2 (somofilcon A) (Device)
结局指标
主要结局
Subjective Overall Score
时间窗: At the end of 15 minutes of daily wear
The primary outcome measure for this study is the subjective overall score on a scale of 0-100 (0= Extremely poor, unmanageable, cannot use lenses, 100= Excellent, highly impressed with these lenses overall).
次要结局
- Subjective Vision(At the end of 15 minutes of daily wear)
- Subjective Comfort(At the end of 15 minutes of daily wear)
研究者
研究点 (1)
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