ClinicalTrials.Veeva

Menu

Validation of Portable Monitoring Device for Diagnosing Sleep Apnea

The Chinese University of Hong Kong logo

The Chinese University of Hong Kong

Status

Completed

Conditions

Sleep Apnea

Treatments

Device: ARES (Apnea Risk Evaluation System)

Study type

Observational

Funder types

Other

Identifiers

NCT00628511
6902256

Details and patient eligibility

About

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

Full 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.

Enrollment

175 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients suspected of sleep apnea

Exclusion criteria

  • patient refuse to participate

Trial design

175 participants in 1 patient group

observation
Treatment:
Device: ARES (Apnea Risk Evaluation System)

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems