Validation of a Novel Device for Screening Patients With Symptoms of OSA

Chinese University of Hong Kong1 site in 1 country97 target enrollmentApril 1, 2017

ConditionsSleep Apnea Syndromes

Overview

Phase: Not Applicable
Intervention: Not specified
Conditions: Sleep Apnea Syndromes
Sponsor: Chinese University of Hong Kong
Enrollment: 97
Locations: 1
Primary Endpoint: the concordance of the ring oximetry with PSG as the gold standard
Status: Completed
Last Updated: 7 years ago

Overview Investigators Eligibility Criteria Outcomes Sites Similar Trials

Overview

Brief Summary

An innovative ring type oxymetry will be wore by patient undergoing sleep study to validate it's accuracy and usefulness as a screening device for patients with symptoms of OSA

Registry

clinicaltrials.gov

Start Date

April 1, 2017

End Date

March 31, 2018

Last Updated

7 years ago

Study Type

Observational

Sex

All

Investigators

Sponsor

Chinese University of Hong Kong

Responsible Party

Principal Investigator

To Kin Wang

Doctor

Chinese University of Hong Kong

Eligibility Criteria

Inclusion Criteria

•Patients above 18 years old and below 70 years old, both men and women

Exclusion Criteria

•Patients requiring oxygen therapy or noninvasive ventilation;
•Patients with a diagnosis of chronic obstructive pulmonary disease, chronic heart failure, neuromuscular disease, insomnia, clinical symptoms of parasomnia, periodic limb movement, or narcolepsy.
•Patients on medication known to interfere with heart rate, such as beta-blockers, digoxin or calcium receptor antagonists.