Skip to content
Bored Studies
Recruiting

Closed Loop Oxygen Control in Chronic Obstructive Pulmonary Disease (COPD) Patients Treated With Nasal High Flow in the Hospital

Fisher and Paykel Healthcare · NCT07222410

View Study & Apply (opens in a new tab)

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
Closed Loop Oxygen Control in Chronic Obstructive Pulmonary… (NCT07222410) | Bored Studies