NCT01846195已完成不适用
Clinical Evaluation of the Zynex Blood Volume Monitor (CM-1500) in Healthy Adult Patients During a Blood Draw
Zynex Monitoring Solutions2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2012年6月6日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 50
- 试验地点
- 2
- 主要终点
- Detect by Non-invasive Monitoring a Change in Blood Volume During a Whole Blood Draw
研究概览
简要总结
Non-invasive monitoring to measure changes in blood volume.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Other
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 35 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Healthy volunteers
- •Between 18-35 years of age
- •Weight between 130-200 pounds
排除标准
- •Known cardiac disease
- •Recent caffeine intake
- •Tobacco use in the (4) hours prior to screening
- •Infection
- •Pregnancy
- •Hemoglobin <13.5 g/dl
结局指标
主要结局
Detect by Non-invasive Monitoring a Change in Blood Volume During a Whole Blood Draw
时间窗: At study completion (completion of blood draw)
Detection by non-invasive monitoring a change in blood volume (yes or no) during a whole blood draw
次要结局
未报告次要终点
研究者
研究点 (2)
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