RECRUITINGINTERVENTIONAL
Evaluation of a Novel Auto-Adjusting Positive Airway Pressure Algorithm for the Treatment of Obstructive Sleep Apnea Clinical Study
About This Trial
This study aims to assess the effectiveness of an investigational algorithm in the treatment of obstructive sleep apnea.
Who May Be Eligible (Plain English)
Who May Qualify:
- Participants willing to give written willing to sign a consent form.
- Participants who can read and comprehend English.
- Participants who ≥ 18 years of age
- Participants who have been using a ResMed AirSense 10 or 11 device.
- Participants currently using AutoSet (APAP) mode.
- Participants being established on PAP therapy for the treatment of OSA for approximately \>3 months.
- Participants who can participate in the study for up to 8 weeks.
Who Should NOT Join This Trial:
- Participants using Bilevel flow generators.
- Participants using CPAP, AutoSet for Her
- Participants who are or may be pregnant.
- Participants with a preexisting lung disease/ condition that would predispose them to pneumothorax (for example: COPD, lung cancer; fibrosis of the lungs; recent (\< 2years) case of pneumonia or lung infection; lung injury.
- Participants believed to be unsuitable for inclusion by the researcher.
- Participants who are currently enrolled in other medical clinical studies
Always talk to your doctor about whether this trial is right for you.
Original Eligibility Criteria
View original clinical language
Inclusion Criteria:
* Participants willing to give written informed consent.
* Participants who can read and comprehend English.
* Participants who ≥ 18 years of age
* Participants who have been using a ResMed AirSense 10 or 11 device.
* Participants currently using AutoSet (APAP) mode.
* Participants being established on PAP therapy for the treatment of OSA for approximately \>3 months.
* Participants who can participate in the study for up to 8 weeks.
Exclusion Criteria:
* Participants using Bilevel flow generators.
* Participants using CPAP, AutoSet for Her
* Participants who are or may be pregnant.
* Participants with a preexisting lung disease/ condition that would predispose them to pneumothorax (for example: COPD, lung cancer; fibrosis of the lungs; recent (\< 2years) case of pneumonia or lung infection; lung injury.
* Participants believed to be unsuitable for inclusion by the researcher.
* Participants who are currently enrolled in other medical clinical studies
Treatments Being Tested
DEVICE
Investigational algorithm
Investigational algorithm developed for the treatment of Obstructive Sleep Apnea.
DEVICE
Control algorithm
Released algorithm intended for the treament of Obstructive Sleep Apnea
Locations (1)
ResMed Ltd
Bella Vista, New South Wales, Australia