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Clinical Trial Summary

The purpose of this study is to compare the effects of nasal and oronasal interfaces during ASV treatment on sleep efficiency and sleep architecture. Therefore, patients starting treatment with ASV, will be randomized between two groups. In the first group, patients will use a nasal interface during the first night and an oronasal interface during the second night. In the second group, patients will use an oronasal mask first and a nasal mask during the second night. The results of this trial will have major impact on future clinical practice as it would deliver prediction rules to choose the correct interface immediately.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02919930
Study type Interventional
Source Universitaire Ziekenhuizen Leuven
Contact Dries Testelmans, MD, PhD
Phone 00 32 16 342522
Email dries.testelmans@uzleuven.be
Status Recruiting
Phase N/A
Start date February 2015
Completion date January 2022

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