ACTRN12616000300471进行中（未招募）未知
Safety and efficacy of automated targeting of oxygen therapy in premature infants
Menzies Institute for Medical Research, University of Tasmania0 个研究点目标入组 60 人开始时间: 2016年3月8日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 60
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
- Treatment
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- o limit 至 4 Months（—）
- 性别
- All
入选标准
- •i) Preterm birth at <32 weeks gestation
- •ii) Requirement for non-invasive respiratory support, including continuous positive airway pressure (CPAP), or high flow via nasal cannula (HF).
- •iii ) Either a) requirement for supplemental oxygen at the time of commencing the study, or b) in room air but showing a propensity to hypoxic events with or without apnoea.
- •iv) Research team available to commence recording.
排除标准
- •Currently ventilated or in imminent need of intubation and ventilation
研究者
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