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Belgian Central Sleep Apnea REgistry (B-CARE)
This study evaluates different factors that determine the treatment choice and treatment compliance in patients with central sleep apnea. All patients will receive routine care (registry).
Central sleep apnea (CSA) is characterized by intermittent cessation or decrease of airflow and effort of breathing during sleep. The diagnostic criteria for CSA varies according to the type of CSA (e.g. CSA due to cardiac failure, due to a medication, ...). CSA is defined as: (1) an apnea/hypopnea index ≥ 15 per hour of sleep and (2) the number of central apneas and/or hypopneas is \> 50% of the total number of apneas and hypopneas. Presence of CSA is associated with excessive daytime sleepiness and poor sleep quality. Furthermore, in patients with heart failure, presence of CSA was found to be related to mortality. As yet, however, there is insufficient knowledge on the clinical features, pathophysiological background and consecutive algorithms for treatment. Currently, it is not fully clear whether CSA or the treatment of CSA is related to disease progress. The aim of this trial is to evaluate the current treatment choices for CSA in Belgium and compliance with and effects of these treatments.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
OLV Ziekenhuis
Aalst, Belgium
ZNA Middelheim
Antwerp, Belgium
UZA
Antwerp, Belgium
AZ Sint-Jan
Bruges, Belgium
CHU Saint-Pierre
Brussels, Belgium
Ghent University Hospital
Ghent, Belgium
Jessa Ziekenhuis
Hasselt, Belgium
AZ Groeninge
Kortrijk, Belgium
CH Jolimont
La Louvière, Belgium
UZ Leuven
Leuven, Belgium
Start Date
June 25, 2018
Primary Completion Date
June 25, 2028
Completion Date
June 25, 2028
Last Updated
July 3, 2024
1,500
ESTIMATED participants
No intervention
OTHER
Lead Sponsor
Universitaire Ziekenhuizen KU Leuven
Collaborators
NCT06043830
NCT03421704
Data Source & Attribution
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