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

Inclusion Criteria2

  • Patients with central sleep apnea, not responding to treatment with CPAP
  • Indication for treatment with ASV

Exclusion Criteria1

  • Patients < 18 years old

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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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