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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00635674
Other study ID # OSAMSCPAP
Secondary ID
Status Completed
Phase N/A
First received February 25, 2008
Last updated March 13, 2008
Start date February 2007
Est. completion date February 2008

Study information

Verified date March 2008
Source Pavol Jozef Safarik University
Contact n/a
Is FDA regulated No
Health authority Slovakia: State Institute for Drug Control
Study type Interventional

Clinical Trial Summary

The increased risk of atherosclerotic morbidity and mortality in patients with obstructive sleep apnea (OSA) has been linked to arterial hypertension, insulin resistance, systemic inflammation, and oxidative stress in previous studies.

We aimed to determine the effects of 8-weeks therapy with continuous positive airway pressure (CPAP) on glucose and lipid profile, systemic inflammation, oxidative stress, and the global cardiovascular disease (CVD) risk in patients with severe OSA and metabolic syndrome.


Description:

Patients with obstructive sleep apnea (OSA) are at increased risk of atherosclerotic morbidity and mortality.OSA is associated with the development and/or worsening of arterial hypertension, a traditional risk factor of atherosclerosis.Moreover, OSA has been linked to novel factors related to atherogenesis - metabolic syndrome,systemic inflammation,6 and oxidative stress.

Numerous studies have selectively examined the effects of continuous positive airway pressure (CPAP) ventilation, the primary treatment for OSA, on the traditional and novel risk factors of atherosclerosis. A recent metaanalysis of 16 randomized trials indicated that CPAP decreases blood pressure in patients with OSA.9 Furthermore, reductions in serum total cholesterol, C-reactive protein (CRP), tumor necrosis factor-alpha (TNF-alpha), interleukin (IL)-6 and IL-8 were demonstrated after effective CPAP therapy.In addition, CPAP was shown to reduce systemic oxidative stress.Improvements in insulin sensitivity have been reported in some,but not in all studies. Importantly, substantial evidence links the effects of CPAP to compliance with this treatment.

Most observational studies examined the effects of CPAP across a broad-range of OSA severity, and have included patients with and without the metabolic syndrome. Up to now, no study analyzed the effects of CPAP on glucose and lipid metabolism, systemic inflammation, oxidative stress, and the global cardiovascular disease (CVD) risk within the same cohort of subjects with severe OSA and concurrent metabolic syndrome. Importantly, the metabolic syndrome exacerbates CVD risk over and above that attributable to OSA alone. Therefore, reduction of CVD risk in patients with OSA and concurrent metabolic syndrome is of paramount importance.

The primary purpose of the present study was to determine, in patients with severe OSA and metabolic syndrome compliant to CPAP, the effects of 8-weeks therapy on the glucose and lipid profile, systemic inflammation, oxidative stress, and on the global CVD risk. The secondary goal was to analyze factors related to compliance with CPAP.


Recruitment information / eligibility

Status Completed
Enrollment 32
Est. completion date February 2008
Est. primary completion date February 2008
Accepts healthy volunteers No
Gender Both
Age group 35 Years to 75 Years
Eligibility Inclusion Criteria:

- severe OSA (more than 30 obstructive apneas or hypopneas per hour of sleep and excessive daytime sleepiness)

- metabolic syndrome

Exclusion Criteria:

- endocrine or metabolic disorders other than metabolic syndrome

- history of myocardial infarction, angina or stroke

- inflammatory or other chronic disease

- respiratory disorder other than OSA

- neurological lesions

- regular use of sedative medication or alcohol

Study Design

Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Intervention

Device:
CPAP device - REMstar Plus, Respironics, Murrysville, USA
continuous positive airway pressure device with heated humidification

Locations

Country Name City State
Slovakia Medical Faculty, PJ Safarik University Kosice

Sponsors (1)

Lead Sponsor Collaborator
Pavol Jozef Safarik University

Country where clinical trial is conducted

Slovakia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Cardiovascular disease risk profile (as assessed using the multivariable risk factor algorithm) 8 weeks therapy with Continuous positive airway pressure No
Secondary insulin sensitivity 8 weeks No
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