ACTRN12616001174471已完成未知
Efficacy of nasogastric and endotracheal tube securement devices, preventative dressings and topical skin applications for reducing device-related pressure injuries in intensive care patients; a pilot study
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 100
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Prevention
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •All ICU patients = or >18 years who have a NGT and/or ETT in situ
- •Patients who are expected to remain in ICU > 24 hours
- •NGT or ETT inserted a maximum of 12 hours prior to ICU admission
- •Patients readmitted to ICU with no oral or nasal skin injury present
- •NGT arm only - must have wide bore NGT and an ETT in situ.
排除标准
- •Burn patients with an ETT wired in place (ETT arm only)
- •Patients with NGT sutured in place or nasal bridle (NGT arm only)
- •Patients with facial trauma
- •Traumatic brain injured patients requiring intracranial pressure monitoring and/or ventricular drainage of cerebrospinal fluid
- •Cervical spine injured patients who have a hard collar in situ
- •Hirsute patients with beards where patient permission to shave is not possible
- •Patients who are receiving non-invasive ventilation
- •Patients with a device (NGT or ETT) predicted to be in situ < 48 hours.
- •Patients with a community or hospital-acquired NGT or ETT PI diagnosed within 24 hours of admission to the ICU.
- •Patients on whom treatment is withdrawn or who are being palliated.
- •Patients currently enrolled on three studies in the ICU.
研究者
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