Interface Selection for Adaptive Servo Ventilation
Recruiting
N/A
Interventional Study
Central Sleep Apnea
ASV
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 15 (estimated)
- Sponsor
- Universitaire Ziekenhuizen KU Leuven · Other
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About This Trial
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 wi…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Patients with central sleep apnea, not responding to treatment with CPAP
* Indication for treatment with ASV
Exclusion Criteria:
* Patients \< 18 years old
Contacts