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Ambulatory Versus Home Blood Pressure Monitoring in Obstructive Sleep Apnea

Conditions
Obstructive Sleep Apnoea
Hypertension
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
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

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

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