NCT07022054已完成不适用
iCare IC1000 Alignment Study
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 100
- 试验地点
- 2
- 主要终点
- Primary Objective
研究概览
简要总结
The primary objective of this study is to evaluate the performance of the alignment feature of iCare IC1000 tonometer.
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
- 是
入选标准
- •Age ≥ 18 years
排除标准
- •Subjects with only one functional eye
- •Central corneal scarring
- •Microphthalmos
- •Buphthalmos
- •Contact lens use during measurement or hard lenses 24h prior to measurement
- •Dry eyes (clinically significant)
- •Keratoconus
- •Any other corneal or conjunctival pathology or infection relevant to this study
- •Coloboma or other pupil deformation
结局指标
主要结局
Primary Objective
时间窗: Through study completion, an average of 2 months
Number of participants with successful intraocular pressure (IOP) measurements using the alignment feature of the iCare IC1000 tonometer during a single clinic visit.
次要结局
未报告次要终点
研究者
研究点 (2)
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