myAirvo 3 (High Flow Nasal Therapy; HFNT) for COPD Patients in the Home
Eligible age
30+ yrs
Accepts
All genders
Locations
14 states
Healthy volunteers
No
See if you qualify for this study
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About this study
Parallel-group, prospective, randomized, controlled phase III trial of home High flow Nasal Therapy (HFNT) via myAirvo 3 plus usual COPD medical care vs. usual COPD medical care, for at least 1 year and up to two years in 642 GOLD Grade D, Stages II-IV patients with moderate to very severe COPD at risk for moderate and severe exacerbations with a prior history of severe exacerbation requiring hospitalization within the past 6 weeks.
Sponsor: Temple University
You may not qualify if…
- ✕ An individual who meets any of the following criteria will be excluded from participation in this study:
- ✕ 1. Current self-reported chronic use of positive airway pressure (PAP) therapy; continuous positive airway pressure (CPAP), or non-invasive positive pressure ventilation (NPPV)
- ✕ 2. A STOPBang Questionnaire score \> 5\*
- ✕ 3. Pregnancy or lactation
- ✕ 4. Treatment with another investigational drug or other intervention within the previous 30 days
- ✕ 5. Life expectancy less than 12 months due to COPD or other comorbid condition.
- ✕ 6. Recent upper airway surgery (within the previous month)
- ✕ 7. Recent head or neck trauma (within the previous month)
Where it's recruiting
Birmingham
Scottsdale
Jacksonville · Kissimmee · Miami · Palmetto Bay
Chicago
West Des Moines
Baltimore
Boston · Burlington
Detroit
Minneapolis
Cincinnati · Cleveland · Columbus
Bethlehem · DuBois · Philadelphia · Pittsburgh
Houston
Source: ClinicalTrials.gov · NCT05204888 · last updated 2025-02-06