NCT06247072已完成不适用
TRK-3 Conformance to Standards for Tonometers
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 125
- 试验地点
- 2
- 主要终点
- IOP
研究概览
简要总结
To collect measurements of a new tonometer and show conformance to standards for tonometers.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 22 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Age at least 22 years at the time of the informed consent
- •Provide voluntary written consent for participation in the study
排除标准
- •Have only one functional eye
- •Have difficulty in ocular fixation or eccentric fixation in either eye
- •Have corneal scar or have a history of corneal surgery such as corneal laser surgery (cataract surgery is acceptable)
- •Have microphthalmia
- •Have buphthalmos
- •Wear contact lens (have used soft contact lenses within the last 3 months and/or hard contact lenses within the last 6 months)
- •Have dry eyes and taking prescription medication or using artificial tears daily
- •Have blepharospasm
- •Have nystagmus
- •Have keratoconus
- •Have corneal or conjunctival lesions or infections
- •Have a central corneal thickness of <500μm or >600μm
- •Have corneal astigmatism >3D
- •Have known allergy to ophthalmic anesthetics
- •Have known allergy to sodium fluorescein
结局指标
主要结局
IOP
时间窗: 1 day
pressure inside the eye
次要结局
未报告次要终点
研究者
研究点 (2)
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