NCT01834612已完成1 期
Clinical Evaluation of the Zynex Blood Volume Monitor (CM1500) in Healthy Adult Volunteers During a Blood Draw
Zynex Monitoring Solutions2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2013年1月7日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 20
- 试验地点
- 2
- 主要终点
- Detect change in blood volume by non-invasive monitoring during whole blood draw
研究概览
简要总结
To determine if a manual blood loss can be detected using the non-invasive blood monitor.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Diagnostic
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 50 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •healthy volunteer
- •between 18 to 50 years of age
- •weight between 157 to 220 lbs
排除标准
- •unstable or untreated cardia disease
- •alcohol consumption in 24 hours prior to screening
- •tobacco use in 4 hours prior to screening
- •pregnancy
- •infection
- •Hemoglobin < 12.5 g/dL at time of procedure
结局指标
主要结局
Detect change in blood volume by non-invasive monitoring during whole blood draw
时间窗: 4 months
次要结局
未报告次要终点
研究者
研究点 (2)
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