Hypertension Clinical Trial
Official title:
The Effects of Obstructive Sleep Apnea and Its Intervention on Coronary Heart Disease
NCT number | NCT02059993 |
Other study ID # | SF2009-2012 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | January 2009 |
Est. completion date | December 2013 |
Verified date | July 2020 |
Source | Chinese Pulmonary Vascular Disease Research Group |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Obstructive sleep apnea(OSA) is an important identifiable cause of hypertension. Previous study has suggested that OSA significantly increases cardiovascular morbidity and mortality, especially in patients with pre-existing cardiovascular disease.The standardized treatment of moderate/severe OSA is continuous positive airway pressure (CPAP). Most of short-term trials indicated that CPAP treatment reduced BP in patients with OSA. But relevant studies have a relative short duration with only but few more than one year. In our opinion, they are not sufficient to detect the real effect of CPAP on reduction in BP. Besides, the impact of OSA on metabolic disorder is still unclear.We hypothesized that long-term CPAP treatment could reduce blood pressure and improve metabolic disorder in patients with coronary heart disease (CHD)and OSA.
Status | Completed |
Enrollment | 83 |
Est. completion date | December 2013 |
Est. primary completion date | December 2013 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 45 Years to 75 Years |
Eligibility |
Inclusion Criteria: - men and women, aged 45 to 75 years old - verified diagnosis of hypertension by medical history or receiving antihypertensive drugs - established diagnosis of CHD - at least 3-month optimal treatment for hypertension - moderate or severe OSA Exclusion Criteria: - if they had secondary hypertension - central sleep apneas - history of significant chronic renal, or hepatic failure or severe pulmonary disease - diagnosed with malignant cancer with a life expectancy of less than 2years - regular use of medications that can affect BP(including corticosteroids or sedative drugs) - severe psychiatric disease - sustained excessive alcohol use - current use of CPAP treatment for OSA or pharyngeal surgery for OSA - New York Heart Association Class III-IV degree - declined to participate or were unable to give informed consent |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Chinese Pulmonary Vascular Disease Research Group |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Cardiovascular and Cerebrovascular Events | Baseline, 1 month, 3 month, 6 month, 12 month, 18 month, 24 month, 30 month, 36 month | ||
Primary | Change of Daytime Systolic Blood Pressure (SBP) and Diastolic Blood Pressure (DBP) Pre-treatment and Post-treatment | baseline and follow-up at 36 months | ||
Secondary | Change in Epworth Sleepiness Scale (ESS) | The epworth sleepiness scale(ESS) measures a person's general level of daytime sleepiness, or their average sleep propensity in daily life (ASP). It is a simple questionnaire based on retrospective reports of the likelihood of dozing off or falling asleep in a variety of different situations. The ESS is the most commonly used method for measuring a person's ASP.The ESS ranges from 0-24, higher scores indicate more severe daytime sleepiness. | baseline,end of study ( up to 54 months) |
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