A Development Study to Evaluate a Nasal Mask for the Treatment of Obstructive Sleep Apnea
- Conditions
- Obstructive Sleep Apnea
- Registration Number
- NCT03124069
- Lead Sponsor
- Fisher and Paykel Healthcare
- Brief Summary
This investigation is designed to evaluate the comfort, ease of use and performance of a trial nasal mask for the treatment of Obstructive Sleep Apnea (OSA) in the home environment.
- Detailed Description
The investigation is a prospective, non-randomized, non-blinded study. Up to 45 OSA patients who currently use a nasal or nasal pillows mask will be recruited
This study will involve a baseline (Visit One) data gathering with the participant's PAP therapy and their usual mask. This will be followed by the participants being fitted with the trial nasal mask for use in-home (Visit Two). The participant then will come in to return the mask (Visit Three) and give feedback on their experience using the mask in home in the form of a structured interview during Visit Three. The maximum amount of time the participants will be exposed to the trial mask in-home will be 14 ± 5 days from Visit Two.
The mask and CPAP (if used from the loan research pool) will be returned to the institution at the conclusion of the trial and participant will return to their usual mask and therapy device for the treatment of Obstructive Sleep Apnea.
Neither the investigators nor the participants will be blinded to the study.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 37
- AHI ≥ 5 from diagnostic PSG night
- Aged 22 and over (FDA defined as adult)
- Either prescribed APAP, CPAP or Bi-Level PAP for OSA
- Existing nasal or nasal pillows mask users (preferable 70%:30% split)
- Fluent in spoken and written English
- Inability to give informed consent
- Patient intolerant to CPAP therapy
- Anatomical or physiological conditions making PAP therapy inappropriate
- Current diagnosis of respiratory disease or CO2 retention
- Pregnant or think they may be pregnant
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Primary Outcome Measures
Name Time Method Number of Participants Subjective Performance Rating of the Nasal Mask 14 ± 5 days In-Home Performance reported from participants questionnaires to evaluate the use of the F\&P nasal mask for treatment of Obstructive Sleep Apnea
Number of Participants Subjective Reporting of Nasal Mask Usability During Visit Two - 20 minutes Usability reported from participants questionnaires to evaluate the use of the F\&P nasal mask for treatment of Obstructive Sleep Apnea
Number of Participants Reporting Comfort Compared to Their Usual Mask. 14 ± 5 days In-Home Comfort reported from participants questionnaires to evaluate the use of the F\&P nasal mask for treatment of Obstructive Sleep Apnea
Number of Participants PAP Device Performance Reporting 14 ± 5 days In-Home Determined from data recorded from the PAP device to evaluate the use of the F\&P nasal mask for treatment of Obstructive Sleep Apnea
Number of Participants Subjective Recording of Ease of Nasal Mask Use. 14 ± 5 days In-Home Ease of use reported from participants questionnaires to evaluate the use of the F\&P nasal mask for treatment of Obstructive Sleep Apnea
- Secondary Outcome Measures
Name Time Method Number of Participants Leak Compared to Usual Mask 14 ± 5 days In-Home Leak data recorded from PAP device to evaluate the use of the F\&P nasal mask for treatment of Obstructive Sleep Apnea
Number of Participants With Correct Nasal Mask Size Determination 1 day-time appointment (1 hour) Sizing determined from a customized fitting tool to evaluate the use of the F\&P nasal mask for treatment of Obstructive Sleep Apnea
Trial Locations
- Locations (1)
Clinical Trials of Florida
🇺🇸South Miami, Florida, United States
Clinical Trials of Florida🇺🇸South Miami, Florida, United States