ACTRN12619000323123已完成不适用
A prospective open label non-randomised study to Investigate the safety of a gas flow failure detection device (SureflO2™ oxygen mask) in elective surgical patients.
VPAS Group Pty Ltd0 个研究点目标入组 249 人开始时间: 2019年3月4日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 249
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
- Non-randomised 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 operative patients scheduled for procedures requiring general anaesthesia OR sedation (in association with local/regional/neuraxial anaesthetic techniques)
- •* Any patient requiring perioperative oxygen supplementation via medium concentration oxygen mask
- •* Elective planned surgical patients (no emergencies or non-elective cases).
排除标准
- •* Patients under 18 or over 18 and not capable of consent
研究者
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