ApneaLink Air Home Sleep Testing (HST) Device Validation Study

Completed · Not applicable

Conditions studied: Sleep-disordered Breathing

In brief

This study compares the diagnostic capability of a home sleep apnea testing device to polysomnography.

Key facts

Study ID

NCT03470493

Run by

ResMed

People needed

130

Starts

2018-04-11

Expected to finish

2019-07-31

Last updated by the study team

2021-05-20

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Participant is 18 years of age or older
• Participant is willing to provide informed consent
• Participant is willing to participate in all study related procedures

You may not qualify if…

• Unable to cease positive airway pressure (PAP) therapy during PSG (if currently using)
• Requires use of oxygen therapy during sleep
• Diagnosis of uncontrolled clinically relevant sleep disorder (e.g., untreated insomnia or restless leg syndrome)
• Pregnant
• Participant is unsuitable to participate in the study in the opinion of the investigator

Where it is running

• University of Florida — Gainesville, Florida, United States
• University of Miami — Miami, Florida, United States

Full record on ClinicalTrials.gov

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