Interface Selection for Adaptive Servo Ventilation
Interface Selection for Adaptive Servo Ventilation: A Randomized Controlled Study
Universitaire Ziekenhuizen KU Leuven
15 participants
Feb 1, 2015
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
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
One night of ASV treatment with oronasal mask followed by one night of ASV treatment with nasal mask.
One night of ASV treatment with nasal mask followed by one night of ASV treatment with oronasal mask.
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT02919930