Validation of Portable Monitoring Device for Diagnosing Sleep Apnea
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|ClinicalTrials.gov Identifier: NCT00628511|
Recruitment Status : Completed
First Posted : March 5, 2008
Last Update Posted : February 9, 2016
|Condition or disease||Intervention/treatment|
|Sleep Apnea||Device: ARES (Apnea Risk Evaluation System)|
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.
|Study Type :||Observational|
|Actual Enrollment :||175 participants|
|Official Title:||A Validation Study of A New Diagnostic Device for Screening of Obstructive Sleep Apnea in High Risk Patient Population|
|Study Start Date :||January 2007|
|Actual Primary Completion Date :||December 2007|
|Actual Study Completion Date :||February 2008|
Device: ARES (Apnea Risk Evaluation System)
application of portable monitoring device with PSG
- validity of portable monitoring device [ Time Frame: 1 year ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00628511
|The Chinese Univerisity of Hong Kong|
|Hong Kong, China|
|Principal Investigator:||To K Wang, MBCHB||Chinese University of Hong Kong|