Assessment of AnchorFast Guard Subglottic ET (Endotracheal) Tube
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 34
- 试验地点
- 8
- 主要终点
- Usability of Study Product
研究概览
简要总结
This study is designed to assess the acceptability and usability of a new Endotracheal Tube (ET) holding device for an orally intubated patient.
详细描述
This is a multiple site prospective assessment of the study product in ICU settings. The study is comprised of each intubated subject wearing one study product until the device either needs to be changed or is no longer required by the subject. The study product is designed to hold a standard or subglottic ET tube and help reduce the potential for occlusion (blockage) of the tube.
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
- 未提供
排除标准
- 未提供
研究组 & 干预措施
New oral endotracheal tube holder
Single Study Product Arm
干预措施: New oral endotracheal tube holder (Device)
结局指标
主要结局
Usability of Study Product
时间窗: At application and product removal (maximum 29 days of patient wearing product)
The usability of the study product at application and at removal.
Overall Acceptability With Study Product
时间窗: At product removal (maximum 29 days of patient wearing product)
The overall acceptability relating to general experience with the study product during use will be rated with a 5-point Likert scale ranging from 1=Very Unacceptable to 5=Very Acceptable
次要结局
未报告次要终点