Closed Loop Oxygen Control in Chronic Obstructive Pulmonary Disease (COPD) Patients Treated With Nasal High Flow in the Hospital
Fisher and Paykel Healthcare · NCT07222410
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 22+ · All sexes
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Not applicable
- Target enrollment
- 70
- US sites recruiting
- 4
- Study start
- January 7, 2026
- Record last updated
- June 23, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
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.
Being studied: Closed loop oxygen control; Manual titration
Conditions: COPD
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
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
Recruiting US locations
The University of Alabama at Birmingham
Birmingham, AL 35294
Site contact: Raymond C Wade · 205-934-2490 · rcwade@uab.edu
Central Iowa Hospital Corp - UnityPoint Health
Des Moines, IA 50309
Site contact: Matthew Trump · 515-205-4013 · mtrump@iowaclinic.com
Icahn School of Medicine at Mount Sinai
New York, NY 10029
Site contact: Kathryn Dubowski · 212-420-2377 · Kathryn.Dubowski@mountsinai.org
Temple University Hospital
Philadelphia, PA 19140
Site contact: Gerard Criner · 215-707-8113 · Gerard.Criner@tuhs.temple.edu
Study contacts (from the official record)
- Jenny Han · 64 9 574 0123 · optio2trial@fphcare.com