ACTRN12619000006145招募中未知
Algorithm feasibility of a novel oxygen delivery system using comfort mode and closed-loop oxygen control in participants with chronic lung disease
Fisher and Paykel0 个研究点目标入组 8 人开始时间: 2019年1月8日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 发起方
- 入组人数
- 8
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
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 o limit(—)
- 性别
- All
入选标准
- •1. Doctor’s diagnosis of a chronic respiratory disease such as COPD, bronchiectasis and Interstitial Lung Disease
- •2. Stable respiratory state with no exacerbation in last 4 weeks
- •1. Doctor’s diagnosis of a chronic respiratory disease such as COPD, bronchiectasis and Interstitial Lung Disease
- •2. Prescribed long term oxygen therapy (LTOT) for use at rest
- •3. Stable respiratory state with no exacerbation in last 4 weeks
- •4. Hypercapnic (PtCO2 >45mmHg), with SpO2 <88% at rest breathing room air OR Normocapnic (PtCO2 less than or equal to 45mmHg), with SpO2<92% at rest breathing room air
排除标准
- •Group A and B
- •1. Age <18
- •2. Cognitive impairment
- •3. Diagnosis of a notifiable disease (eg. hepatitis, TB, rheumatic fever, HIV, gastroenteritis)
- •4. The presence of an implantable Medical Device (eg. pacemaker, defibrillator, neurostimulator or insulin pump)
- •5. Known infection or colonization with multidrug resistant bacteria, Pseudomonas species, Burkholderia Cepacia or mycobacteria
- •6. The presence of an implantable Medical Device (eg. Pacemaker, defibrillator, neurostimulator, or insulin pump).
- •7. Any other condition which, at the investigator’s discretion, is believed may present a safety risk or impact the feasibility of the study or the study results.
- •Group B ONLY
- •1. Inability to tolerate an interruption in oxygen therapy
- •2. Requirement for more than 4L/min LTOT at rest
研究者
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