Interface Selection for Adaptive Servo Ventilation

Status Recruiting

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

Clinical Trial Details

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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See also
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