NCT03121144已完成不适用
Usability Validation of Patient Monitoring Device for Pressure Injury Prevention and Fall Detection
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 34
- 试验地点
- 1
- 主要终点
- Usability Validation of Masimo Centroid System
研究概览
简要总结
This study describes a procedure to collect a subject's position, movement, physiological data and usability information using Masimo's investigational device.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Other
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •At least 18 years of age
- •ICU patient
- •Primarily bedbound subjects
- •Able to be monitored for a minimum of approximately 8 hours
排除标准
- •Prisoner status
- •Pressure injury stage 2, 3, or ungroupable
- •Has a pacemaker or internal defibrillator
- •Has a history of complications with a similar study
- •Has any medical condition which in the judgment of the Investigator, renders them inappropriate for participation in this study
研究组 & 干预措施
Masimo Centroid System
Experimental
Single-arm study. All subjects are enrolled into the test group wherein the noninvasive positional monitoring device will be administered.
干预措施: Masimo Centroid System (Device)
结局指标
主要结局
Usability Validation of Masimo Centroid System
时间窗: At least 8 hours
The number of participants enrolled to assess the usability of the Masimo Centroid System.
次要结局
未报告次要终点
研究者
研究点 (1)
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