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A Study to Determine Preferences Towards Interface Products

Sleep Disorder; Breathing-Related Clinical Trial

Official title:
A Study to Determine Clinician and Patient Preferences Towards Interface Products Recommended by the 3D Mask Advice Tool

Clinical Trial Summary

Enrolled Naïve participants will be randomized to one of two arms, the investigational or control arm. Once randomized the institutions will fit the participant with the procedures outlined in the protocol. Each participant will be required to trial the mask for a period of 90 days. Any Unscheduled Visits or Calls that occur during the participants 90 days documented.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03948152
Study type Interventional
Source Philips Respironics
Contact
Status Completed
Phase N/A
Start date April 18, 2019
Completion date February 7, 2020
View Details
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