Nebula Study - Screener Apps and HSAT vs. PSG Comparison

Completed · Not applicable

Conditions studied: Sleep Apnea, Obstructive

In brief

This is a prospective, unblinded, open-label, single group study. All subjects will undergo concurrent screener app, HSAT testing, and in-lab polysomnography.

Key facts

Study ID

NCT04597749

Run by

ResMed

People needed

50

Starts

2020-10-27

Expected to finish

2021-01-20

Last updated by the study team

2021-02-04

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: 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 PAP therapy during PSG (if currently using)
• Requires use of oxygen therapy during sleep
• Diagnosis of untreated clinically relevant sleep disorder (other than SDB)
• Pregnant
• Participant is unsuitable to participate in the study in the opinion of the investigator
• Participant has a permanent pacemaker, sustained non-sinus cardiac arrhythmias, and/or takes alpha blocker or short acting nitrate medication.

Where it is running

• Clayton Sleep Institute — Maplewood, Missouri, United States

Full record on ClinicalTrials.gov

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