This investigation is a prospective, non randomized, non blinded study. This investigation is designed to evaluate the performance, comfort and ease of use with the F\&P trial nasal pillows mask amongst Obstructive Sleep Apnea (OSA) participants.
Visit 1 will involve the participants consented in to the trial. Participants will be fitted with the F\&P trial nasal pillows mask for use in-lab. The participant will then return the mask and have a interview, this ensures the maximum time participants will be exposed to the trial mask in lab will be in 1 night. The mask will be returned to the Institution at the conclusion of the trial and the participant will return to their previous mask. The Institution will recruit all participants within 1 week of the beginning of the study.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
9
Investigative Nasal pillows Mask to be used for OSA therapy
Fisher & Paykel Helathcare
Auckland, New Zealand
Ease of use
Subjective Questionnaire
Time frame: 1 night
Acceptability
Subjective Questionnaire
Time frame: 1 night
Objective Leak Data
Data obtained from participant's device - Objective
Time frame: 1 night
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