Validation of Portable Monitoring Device for Diagnosing Sleep Apnea

A Validation Study of A New Diagnostic Device for Screening of Obstructive Sleep Apnea in High Risk Patient Population

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT00628511

Enrollment

175

Registered

2008-03-05

Start date

2007-01-31

Completion date

2008-02-29

Last updated

2016-02-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sleep Apnea

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.

Interventions

DEVICEARES (Apnea Risk Evaluation System)

application of portable monitoring device with PSG

Eligibility

Sex/Gender

ALL

Healthy volunteers

Inclusion criteria

* patients suspected of sleep apnea

Exclusion criteria

* patient refuse to participate

Design outcomes

Primary

Measure	Time frame
validity of portable monitoring device	1 year

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026