Monitor Patients With Sleep Apnea
Completed
- Conditions
- Sleep Apnea
- Registration Number
- NCT00918502
- Lead Sponsor
- Corventis, Inc.
- Brief Summary
The primary objective of the study is to gather data to correlate physiological signals measured by the AVIVO™ Mobile Patient Management System with the patient's respiratory status, including apnea and hypopnea events, during polysomnography
- Detailed Description
Patients with suspected sleep disordered breathing will be monitored during polysomnography and the collected information will be used to assess patient's respiratory status.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
- Is female or male, 18 years of age or older
- Undergoing polysomnography for suspected sleep apnea
- Is willing to provide written informed consent and comply with study guidelines
Exclusion Criteria
Not provided
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What physiological signals does the AVIVO™ system use to detect apnea and hypopnea events in sleep apnea patients?
How does the AVIVO™ Mobile Patient Management System compare to standard polysomnography in detecting sleep disordered breathing?
Are there specific biomarkers associated with sleep apnea severity that the AVIVO™ system can identify during monitoring?
What are the potential adverse events associated with using the AVIVO™ system for respiratory monitoring in sleep apnea studies?
What is the role of respiratory signal analysis in improving patient outcomes for obstructive sleep apnea using the AVIVO™ system?