NCT02198560已完成不适用
RS-3000 Lite Agreement Study
Nidek Co. LTD.1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2014年8月最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- Retinal thickness and Optic Disc Analysis
研究概览
简要总结
The primary objectives of the study are to assess the agreement between the two different scan mode of the RS-3000 Lite.
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
- 20 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Subjects who do not have pathology in both eyes
排除标准
- •Subjects who have any of the following conditions:
- •Diabetes mellitus (DM) and/or diabetic retinopathy
- •Uncontrolled Hypertension (HT)
- •Cerebral infarction, cerebral hemorrhage, cranial nerve neoplasm and other central nervous system diseases affecting vision
- •Cardiac, hepatic, renal and hematologic diseases
- •A current condition requiring systemic administration of steroid
- •A history of, or currently receiving, anticancer therapy
- •Epileptic seizures which are optically induced
- •Note: Additional criteria may apply
结局指标
主要结局
Retinal thickness and Optic Disc Analysis
时间窗: 3 hours
Time frame is the maximum duration of hospital stay.
次要结局
- Number of participants with adverse events(1day)
研究者
研究点 (1)
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