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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
Sponsor:
Information provided by:
Chinese University of Hong Kong

Brief Summary:
portable monitoring device could diagnose sleep apnea in high risk patients.

Condition or disease Intervention/treatment
Sleep Apnea Device: ARES (Apnea Risk Evaluation System)

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.


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

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Sleep Apnea
U.S. FDA Resources

Group/Cohort Intervention/treatment
observation Device: ARES (Apnea Risk Evaluation System)
application of portable monitoring device with PSG



Primary Outcome Measures :
  1. validity of portable monitoring device [ Time Frame: 1 year ]


Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
patients suspected of sleep apnea
Criteria

Inclusion Criteria:

  • patients suspected of sleep apnea

Exclusion Criteria:

  • patient refuse to participate

Information from the National Library of Medicine

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


Locations
China
The Chinese Univerisity of Hong Kong
Hong Kong, China
Sponsors and Collaborators
Chinese University of Hong Kong
Investigators
Principal Investigator: To K Wang, MBCHB Chinese University of Hong Kong

Responsible Party: To K W, The Hospital Authority
ClinicalTrials.gov Identifier: NCT00628511     History of Changes
Other Study ID Numbers: 6902256
First Posted: March 5, 2008    Key Record Dates
Last Update Posted: February 9, 2016
Last Verified: February 2008

Additional relevant MeSH terms:
Apnea
Sleep Apnea Syndromes
Respiration Disorders
Respiratory Tract Diseases
Signs and Symptoms, Respiratory
Signs and Symptoms
Sleep Disorders, Intrinsic
Dyssomnias
Sleep Wake Disorders
Nervous System Diseases