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Recruiting
NCT07826429
Evaluation of the F&P Mask, US, 2026
Conditions: Chronic Respiratory Conditions, Obstructive Sleep Apnea (OSA)
Sex: All
Ages: 22 Years – N/A
Healthy volunteers: No
Phase: NA
Enrollment: 45
Sponsor: Fisher and Paykel Healthcare
Location: Clayton Sleep Institute St Louis Missouri
Summary
This clinical investigation is designed to validate and confirm the overall performance, safety, usability, reliability, and acceptability of the F\&P Licorice mask in a home environment.
Eligibility Criteria
Inclusion Criteria:
* Are ≥22 years of age
* Weigh ≥66 pounds
* Have been prescribed PAP/NIV therapy by a physician
* Are an existing PAP/NIV therapy mask user with ≥3 months of use prior to enrolment in the clinical investigation\*
* Are compliant with PAP/NIV therapy for ≥4 hours per night for ≥70% of nights for a 14-day period within 30 days prior to enrolment in the clinical investigation
* Are fluent in spoken and written English
* Possess the capacity to provide informed consent
Exclusion Criteria:
* Are intolerant to PAP/NIV therapy
* Possess, or suffer from, anatomical or physiological conditions which make PAP/NIV therapy inappropriate
* Are required to use PAP/NIV therapy for \>12 hours per day or for extensive periods, not including sleep or naps
* Are trying to get pregnant, are pregnant, or think they may be pregnant
* Have an IPAP pressure of \>30 cmH2O if on BPAP
* Use a PAP/NIV therapy device for the delivery of medicines, except supplemental O2
* Use a PAP/NIV therapy device that does not possess data recording capabilities to capture AHI and a numerical indicator of leak that is accessible to the clinical investigation site
* Have a history of light-induced seizures (for optional anthropometric scan only)
Source: ClinicalTrials.gov (NCT07826429). StuddyBuddy aggregates publicly available trial information.