ACTRN12619000006145
Recruiting
N/A
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 sites8 target enrollmentJanuary 8, 2019
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- COPD
- Sponsor
- Fisher and Paykel
- Enrollment
- 8
- Status
- Recruiting
- Last Updated
- 5 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •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
Exclusion Criteria
- •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
Outcomes
Primary Outcomes
Not specified
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