The Evaluation of a Mask for the Treatment of Obstructive Sleep Apnea

Status Completed

Clinical Trial Summary

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 full face and nasal mask amongst Obstructive Sleep Apnea (OSA) patients. Up to 70 OSA patients will be recruited from the North Texas Lung and Sleep Clinic (NTLSC) database

Clinical Trial Description

Visit 1 will involve the participants being fitted with the F&P trial full face or nasal mask for use in-home. The participant will then come in to return the mask (Visit Two) and have a final interview, this ensures the maximum time participants will be exposed to the trial mask in home will be 14 ± 4 days from visit one. 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 patients within three weeks of the beginning of the study. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03142438
Study type	Interventional
Source	Fisher and Paykel Healthcare
Contact
Status	Completed
Phase	N/A
Start date	May 30, 2017
Completion date	June 23, 2017

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