Brigham and Women's Hospital
Boston, Massachusetts, 02115, United States
Location status: Recruiting
NCT Number: NCT07062770
The goal of this research is to better understand how different CPAP mask designs affect airflow and rebreathing of exhaled carbon dioxide (CO₂) during sleep in individuals with obstructive sleep apnea (OSA).
Interested in participating?
Request Info21 year–70 year
All sexes
Interventional
Not applicable
Boston, Massachusetts, 02115, United States
Location status: Recruiting
To understand the existence and severity of circuit rebreathing during treatment with continuous positive airway pressure (CPAP) using different sizes of the exhaust ports in individuals with obstructive sleep apnea (OSA).
Flow-adjusted end-tidal oxygen (PetO2) and carbon dioxide (PetCO2) will be assessed to determine the magnitude of hypoxic load during both wakefulness and sleep. To systematically assess these conditions, the conditions were defined as follows:
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Subjects will be administered either 0, 5 or 10 cmH2O
Subjects will be administered varying levels of exhaust flow: 35, 23, 18, 13 and 8 L/s
Time frame: through study completion, an average of 1 year
Difference in FiO2 between 23L/s vs 13L/s exhaust flow at 5 cmH2O PAP.
Time frame: through study completion, an average of 1 year
Difference in FiO2 between 23L/s vs 13L/s exhaust flow at 5 cmH2O PAP.
Time frame: through study completion, an average of 1 year
Difference in hyboxic burden between 23L/s vs 13L/s exhaust flow at 5 cmH2O PAP.
Interested in participating?
Request InfoBrigham and Women's Hospital
Other
Assessment of Circuit Rebreathing During Continuous Positive Airway Pressure (CPAP) Therapy
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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