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临床试验/ACTRN12619000006145
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

发起方
Fisher and Paykel

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