Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Philips Respironics
Age
21–85
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Adult Volunteers (ages 21-85)
Willing and able to provide informed consent
Able to follow instructions
Able to read and speak in English as their primary language
Currently diagnosed with Sleep Apnea through an in-lab sleep (polysomnography (PSG)) or home sleep testing, but has not started therapy and/or been fit with a mask.
You may not be if
Pre-existing conditions such as bullous lung disease, pathologically low blood pressure, bypassed upper airway, pneumothorax, pneumocephalus, cerebral spinal fluid (CSF) leaks, cribriform plate abnormalities, and prior history of head trauma that has resulted in current cognitive dysfunction.
Prescribed an Adaptive Servo Ventilation (ASV) device
The presence of physical or mental limitations that would limit the ability to test the mask.
Obstructive Sleep Apnea (OSA) diagnosis achieved through a split night sleep study
Known allergy to silicone
Unique facial features (i.e. deformities of the face and/or head, piercings, etc) that could interfere with the use of masks.
Employee of Philips or spouse of a Philips employee
Currently participating in another interventional research study or planned participation in another interventional research study during the trial period (by self-report)
Surgery involving the eyes, ears, nose, sinuses, or upper airway within the last 90 days.
Planned surgical procedures involving the head, neck, face (eyes, ears, nose), or lung during the trial period.
Uncontrolled or poorly managed gastroesophageal reflux
Impaired cough reflex
Untreated or symptomatic hiatal hernia
Untreated glaucoma
Untreated chronic dry eyes
Unable to remove the sleep apnea mask without the assistance of others
Use of prescription drugs that induce vomiting
Clareo Health | A Study to Determine Preferences Towards Interface Products
