ACTRN12614000311651已完成未知
An evaluation involving an in-lab assessment and an in-home trial comparing a modified continuous positive airway pressure device to a comparable market-released continuous positive airway pressure device in terms of treatment efficacy for treating Obstructive Sleep Apnea and comfort.
Hanie Yee0 个研究点目标入组 100 人开始时间: 2014年3月24日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 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
- Treatment
- 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
- •Diagnosed with OSA by a practicing sleep physician
排除标准
- •Patients that have used CPAP with pressure relief in the last two years, to prevent bias towards their current device.
- •Patients with a known history of Cerebrospinal fluid leak, abnormalities of the cribriform plate, head trauma and/or pneumocephalus
- •Patients with pathologically low blood pressure, pneumothorax, a previous history of pneumothorax, or for patients who have an increased risk of pneumothorax, such as those with bullous lung disease
- •Patient with bypassed upper airway
- •Patients with COPD or respiratory failure
- •Patients that require supplemental oxygen with their CPAP device
- •Patients with implanted electronic medical devices (e.g. cardiac pacemakers), to prevent interfernce with/by trial machine
研究者
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