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Clinical Trial Summary

Prospective, follow-up registry of heart failure patients with or without sleep-disordered breathing (SDB). To test the hypothesis that treatment of nocturnal central sleep apnea with Cheyne-Stokes respiration by adaptive servoventilation (ASV) improves symptoms, cardiac performance and event-free survival.


Clinical Trial Description

The study is intended to investigate therapeutic effects of adaptive servoventilation in patients with sleep-disordered breathing and chronic heart failure. These effects include short-/long-term effects on

- symptoms and quality of life

- physical and cardiac performance (6min walking test, cardiopulmonary exercise testing)

- echocardiographic parameters

- arrhythmias

- NT-proBNP

- Respiratory stability (blood gases, rebreathing test, VE/VCO2-slope in cardiopulmonary exercise testing)

- Compliance with ASV therapy

- Event free survival (death, heart transplantation, assist device implantation)

All of these data are also obtained in patients who basically meet the inclusion criteria but in whom sleep-disordered breathing was excluded by means of cardiorespiratory polygraphy or polysomnography and in patients with sleep-disordered breathing who do not undergo adaptive servoventilation for various reasons. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01657188
Study type Observational
Source Ruhr University of Bochum
Contact
Status Completed
Phase
Start date May 2009
Completion date December 2017

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