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Clinical Trial Details — Status: Completed

Administrative data

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

Study information

Verified date July 2020
Source Chinese Pulmonary Vascular Disease Research Group
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Description:

Obstructive sleep apnea (OSA) is a common disorder characterized by repetitive partial (hypopnea) or complete (apnea) occlusion of the upper airway during sleep caused by collapse of the pharyngeal airway, resulting in sleep fragmentation and oxyhemoglobin desaturation. Kiely and colleague's study showed that over 20% of hypertensive patients exhibit OSA, whereas prevalence of hypertension in the setting of OSA exceeds 50%. One study confirmed that OSA is an important identifiable cause of hypertension. OSA is considered as one of the most common risk factors of resistant hypertension. Previous study has suggested that OSA significantly increases cardiovascular morbidity and mortality, especially in patients with pre-existing cardiovascular disease. Several studies confirmed that CPAP reduced systolic blood pressure (SBP) and diastolic blood pressure (DBP) in patients with OSA. Additionally, some papers reported that there was a protective effect of CPAP therapy against death from cardiovascular disease in patients with severe OSA. Other researches regarding the antihypertensive effect of CPAP therapy, however, showed that CPAP had no antihypertensive effect. 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. According to our knowledge, there is no report about long-term effect of CPAP on BP in hypertensive patients with coronary revascularization (CRV) and OSA under conventional antihypertensive medications. Therefore, we conducted a long-term, prospective controlled study to investigate the effects of CPAP on BP, metabolic disorder, clinical symptoms, cardiovascular and cerebrovascular events in patients with CHD and OSA on conventional treatment.


Recruitment information / eligibility

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

Study Design


Intervention

Device:
continuous positive airway pressure
mean continuous positive airway pressure use was at least 4 hours per night;continuous positive airway pressure group received fixed-level continuous positive airway pressure titration using an automated pressure

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Chinese Pulmonary Vascular Disease Research Group

Outcome

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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