Validation of Portable Monitoring Device for Diagnosing Sleep Apnea
Completed
- Conditions
- Sleep Apnea
- Interventions
- Device: ARES (Apnea Risk Evaluation System)
- Registration Number
- NCT00628511
- Lead Sponsor
- Chinese University of Hong Kong
- Brief Summary
portable monitoring device could diagnose sleep apnea in high risk patients.
- Detailed Description
This is a pilot study of another larger cohort investigating different algorithms in managing patients suspected of sleep apnea using portable monitoring device.
Portable monitoring device is applied simultaneously with PSG to compare it's accuracy and validity.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 175
Inclusion Criteria
- patients suspected of sleep apnea
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Exclusion Criteria
- patient refuse to participate
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Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description observation ARES (Apnea Risk Evaluation System) -
- Primary Outcome Measures
Name Time Method validity of portable monitoring device 1 year
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
The Chinese Univerisity of Hong Kong
🇨🇳Hong Kong, China