Ambulatory Versus Home Blood Pressure Monitoring in Obstructive Sleep Apnea
- Conditions
- Obstructive Sleep ApnoeaHypertension
- Registration Number
- NCT01685736
- Lead Sponsor
- University of Athens
- Brief Summary
Subjects referred to a sleep clinic had polysomnography (PSG), clinic BP measurements, 24-hour ABP monitoring and HBP monitoring using a device (Microlife WatchBP HomeN) that allows daytime (3 days, 2 duplicate readings/day) and automated nighttime BP measurement (3 nights, 3 readings/night).
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
- Age ≤ 65 years
- Suspected OSA
- Treated or untreated for hypertension
Exclusion Criteria
- History of cardiovascular disease (heart failure, coronary heart disease, arrhythmia or stroke)
- History of asthma or chronic obstructive pulmonary disease (FEV1/FVC <70%)
- History of diabetes mellitus, collagen diseases and sarcoidosis
- Serum creatinine >1.6 mg/dl, proteinuria
- Previous treatment with CPAP
- Pregnancy or menstruation during the study
- Treatment with steroids, lithium or any other drugs affecting BP
- Change in antihypertensive treatment(if any) in the last 8 weeks before study entry
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (2)
Hypertension Center, Third Department of Medicine, University of Athens, Greece
🇬🇷Athens, Greece
First University Department of Respiratory Medicine, Sotiria Hospital
🇬🇷Athens, Greece