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RECRUITING
NCT02919930
NA

Interface Selection for Adaptive Servo Ventilation

Sponsor: Universitaire Ziekenhuizen KU Leuven

View on ClinicalTrials.gov

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.

Official title: Interface Selection for Adaptive Servo Ventilation: A Randomized Controlled Study

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

15

Start Date

2015-02

Completion Date

2025-01

Last Updated

2024-07-03

Healthy Volunteers

No

Interventions

DEVICE

Switch from oronasal to nasal mask during ASV treatment

One night of ASV treatment with oronasal mask followed by one night of ASV treatment with nasal mask.

DEVICE

Switch from nasal to oronasal mask during ASV treatment

One night of ASV treatment with nasal mask followed by one night of ASV treatment with oronasal mask.

Locations (1)

UZ Leuven

Leuven, Belgium