NCT01298479已完成不适用
Quantitative Determination of the Volume of Suspension Delivered Via the Uniject Delivery System Following Simulated Subcutaneous Injection by Healthcare Professionals Into a Synthetic Subcutaneous Injection Training Device
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- Pfizer
- 入组人数
- 25
- 试验地点
- 1
- 主要终点
- Weight of drug suspension delivered (estimated by change in mass of the Uniject(TM) delivery system).
研究概览
简要总结
The purpose of this study is to determine the volumetric delivery of the Uniject.
详细描述
Observe subjects deliver the drug None used
研究设计
- 研究类型
- Observational
- 观察模型
- Other
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- 未提供
排除标准
- •Non-nurses
结局指标
主要结局
Weight of drug suspension delivered (estimated by change in mass of the Uniject(TM) delivery system).
时间窗: Visit 1
次要结局
未报告次要终点
研究者
研究点 (1)
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