Obstructive sleep apnoea syndrome (OSAS) Respiratory Sleep disorders
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients aged 18 or older 2. Patients with suspicion of obstructive sleep apnoea syndrome or central apnoea events
Exclusion criteria
Exclusion criteria: 1. Mental disorder preventing appropriate judgment concerning study participation 2. Significant co morbidity resulting in reduced life expectancy (lower than 6 months) 3. Planned emigration or relocation within the country during the study period 4. Pregnancy and breast-feeding
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| 1. Median circulating copeptin, Pro-ANP and Pro-ADM levels before treatment and after 1 and 6 months of treatment respectively 2. Change in median circulating copeptin, Pro-ANP and Pro-ADM levels after 1 night and 6 months of CPAP treatment respectively In a second step, endpoints will be assessed in subgroups of patients according to OSAS severity | — |
Primary
| Measure | Time frame |
|---|---|
| Change in median circulating copeptin, Pro-ANP and Pro-ADM levels after 1 month of CPAP or BiPAP treatment | — |
Countries
Switzerland