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NCT00284037 Clinical Trial

Improvement in Baroreflex Sensitivity in OSAS

Obstructive Sleep Apnea Syndrome Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data
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

Study information
Verified date May 2005
Source Nagoya University
Contact Akiko Noda, PhD
Phone +81-52-719-1537
Email a-noda@met.nagoya-u.ac.jp
Is FDA regulated No
Health authority Japan: Ministry of Health, Labor and Welfare
Study type Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility
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.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Device:
• continuous positive airway pressure therapy

Locations
Country Name City State
Japan Nagoya University of Health Sciences Nagoya

Sponsors (1)
Lead Sponsor Collaborator
Nagoya University

Country where clinical trial is conducted

Japan, 

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