NCT03573635已完成不适用
Evaluation of the Effectiveness and Safety of an Own-invention System for Continuous Supraglottic Aspiration in Intubated and Mechanically Ventilated Patients: the "SUPRAtube" Device
Fundación Cardiovascular de Colombia2 个研究点 分布在 1 个国家目标入组 38 人开始时间: 2016年1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
- 38
- 试验地点
- 2
- 主要终点
- aspirated secretions
研究概览
简要总结
Purpose of the trial: Evaluate the efficacy and safety of the device of self-invention of continuous oropharyngeal aspiration denominated "SUPRAtube" in patients with orotracheal intubation and mechanical ventilation.
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
- •Endotracheal intubation and invasive mechanical ventilation,
排除标准
- •Immediate postoperative oral cavity.
- •Traumatic oral cavity injury.
- •Platelet count less than 50000.
研究组 & 干预措施
Supratube
Other
Patient with orotracheal intubation and supratube device
干预措施: Supratube (Device)
Supratube
Other
Patient with orotracheal intubation and supratube device
干预措施: Reference (Other)
结局指标
主要结局
aspirated secretions
时间窗: 24 hours after intubation
volume of aspirated secretions
次要结局
- Adverse events(24 hours after intubation)
研究者
研究点 (2)
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