RecruitingNot ApplicableNCT02919930

Interface Selection for Adaptive Servo Ventilation

Interface Selection for Adaptive Servo Ventilation: A Randomized Controlled Study


Sponsor

Universitaire Ziekenhuizen KU Leuven

Enrollment

15 participants

Start Date

Feb 1, 2015

Study Type

INTERVENTIONAL

Conditions

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.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a medical device called Switch from nasal to oronasal mask during ASV treatment and a medical device called Switch from oronasal to nasal mask during ASV treatment for people with asv and central sleep apnea. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICESwitch 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.

DEVICESwitch 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

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NCT02919930


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