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Bioburden and Usability Evaluation of a Nasal Prototype CPAP Mask

Obstructive Sleep Apnea Clinical Trial

Official title:
Bioburden and Usability Study of the Geelong Mask System

Clinical Trial Summary

AIM AND HYPOTHESIS: The purpose of this study is to monitor the bioburden and impedance characteristics of a prototype mask system and to evaluate the usability of the mask system. The mask system will be assessed according to objective data recordings and user questionnaires. It is hypothesised that the prototype mask components will not pose a health risk (with regards to bioburden and impedance) and that the mask system will pass usability objectives to adequately deliver CPAP treatment.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02255539
Study type Interventional
Source ResMed
Contact
Status Completed
Phase N/A
Start date January 2015
Completion date March 2015
View Details
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