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WatchPAT Device Validation Study Compared to Polysomnography — WPAT  

Sleep Clinical Trial

Official title:
Validation Study of the WatchPAT 200 in the Diagnosis of Obstructive Sleep Apnea in Children 4-12 Years of Age

Clinical Trial Summary

Validation study of a novel sleep Device compared to a traditional sleep study.

Clinical Trial Description

This is an investigator-initiated validation study for the WatchPAT 200 device compared to the gold standard polysomnography procedure (sleep study). To evaluate the accuracy of the WatchPAT device compared to an in-laboratory Polysomnogram (PSG), measurements including obstructive apnea hypopnea index (OAHI), apnea hypopnea index (AHI), oxygen desaturation index (ODI) and other relevant sleep parameteres and indices will be compared. Ultimately, the diagnostic agreement of the WatchPAT device in detecting between normal sleep and mild sleep apnea architecture will be assessed. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03188718
Study type Interventional
Source University of Colorado, Denver
Contact
Status Completed
Phase N/A
Start date December 7, 2017
Completion date June 1, 2019
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