Closed loop oxygen control: Nasal high flow with closed loop oxygen control
Manual titration: Nasal high flow with manual titration
Study summary
The trial aims to evaluate whether the Airvo 3 device in OptiO2 mode can maintain patients' SpO2 levels within the target range better than manual oxygen titration in hospitalized COPD patients with hypoxemia/respiratory distress.
Eligibility
Sex
ALL
Min age
22 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* Has cognitive ability to provide informed consent
* Aged 22 years or older
* Hospitalized with hypoxemia/respiratory distress
* Diagnosis of COPD
* Candidate for/currently prescribed nasal high flow (flow rate of at least 25 L/min) with supplemental oxygen, as assessed by the investigator
* Expected duration of oxygen and nasal high flow therapy \>24 hours (not necessarily continuous)
Exclusion Criteria:
* Receiving Non Invasive Ventilation (NIV) or indicated for NIV as per European Respiratory Society /American Thoracic Society guidelines
* Hemodynamic instability (systolic blood pressure \<90mmHg or requirement for vasopressor or inotropic support)
* Patient receiving end of life care
* Nasal or facial conditions precluding use of nasal high flow
* Pregnancy or breastfeeding
* Cognitive impairment or impaired consciousness precluding informed consent
* Unsuitable for adhesive finger pulse oximetry, as assessed by the investigator
* Any other condition which, at the investigator's discretion, is believed to present a safety risk to the patient if included
* The presence of any active comorbidities that affect the patient's condition importantly in the next 30 days, as assessed by the investigator
* Has already participated in this clinical trial
Primary outcome measure(s)
Percentage of time with SpO2 in target range over period of observation — 24 hours
Percentage of time with SpO2 out of target range over period of observation — 24 hours
Trial sites (4)
Facility
City
Region
Status
The University of Alabama at Birmingham
Birmingham
Alabama
Recruiting
Central Iowa Hospital Corp - UnityPoint Health
Des Moines
Iowa
Recruiting
Icahn School of Medicine at Mount Sinai
New York
New York
Recruiting
Temple University Hospital
Philadelphia
Pennsylvania
Recruiting
More Fisher and Paykel Healthcare trials in the USA
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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