NCT03628833已完成不适用
Hill-Rom Incontinence Management System ICU Field Evaluation
Hill-Rom2 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2018年7月10日最近更新:
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 10
- 试验地点
- 2
- 主要终点
- Staff satisfaction surveys on product performance
研究概览
简要总结
The objective of this Field Evaluation is to assess usage and satisfaction associated with the Hill-Rom Incontinence Management System.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 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
- •Patients with urinary, fecal, or dual incontinence who are ≥ 18 years old
- •The patient, or the patient's legal authorized representative (LAR), is willing and able to provide written informed consent
排除标准
- •Patients that are considered to be near death or require palliative care
研究组 & 干预措施
Incontinence Management system
Experimental
干预措施: Incontinence Management System (Device)
结局指标
主要结局
Staff satisfaction surveys on product performance
时间窗: Through study completion, an average of 4 months
Following product use, staff can complete an optional, Likert scale survey
次要结局
- Patient exposure time following an incontinence event(Through study completion, an average of 4 months)
研究者
研究点 (2)
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