Obstructive Sleep Apnea Syndrome Clinical Trial
NCT number | NCT00284037 |
Other study ID # | NU-06-A-0003 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | January 27, 2006 |
Last updated | January 27, 2006 |
Individuals with obstructive sleep apnea syndrome (OSAS) are at high risk for cardiovascular morbidity and mortality. The effect of long-term nocturnal therapy with continuous positive airway pressure (CPAP) on daytime baroreflex sensitivity (BRS), a predictor of cardiac death, was investigated in OSAS patients.
Status | Recruiting |
Enrollment | 0 |
Est. completion date | |
Est. primary completion date | |
Accepts healthy volunteers | |
Gender | Both |
Age group | 20 Years to 70 Years |
Eligibility |
Inclusion Criteria: - obstructive sleep apnea syndrome Exclusion Criteria: - diabetes mellitus, chronic obstructive lung disease, coronary or valvular heart disease, congestive heart failure, renal failure, or endocrine dysfunction. Moreover, none of them were taking b-blockers, vasodilators, or inotropic agents at the time of enrollment in the study. |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Japan | Nagoya University of Health Sciences | Nagoya |
Lead Sponsor | Collaborator |
---|---|
Nagoya University |
Japan,
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