Exploration of Current and New Technologies for Accuracy of Diagnosing OSA

Sponsor
ResMed
Study ID
NCT07485582
Status
Not Yet Recruiting

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Conditions

  • Obstructive Sleep Apnea

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Device A — DEVICE
    A finger worn OSA home sleep test (HST) diagnostic device
  • Device B — DEVICE
    A wrist worn OSA home sleep test (HST) diagnostic device
  • Device C — DEVICE
    Ring: wellness device
  • Device D — DEVICE
    Torso and limb worn patches
  • Device E — DEVICE
    An eye mask
  • Screener A — DIAGNOSTIC_TEST
    A mobile app screener

Study Details

Resmed is the manufacturer of medical devices which screen, diagnose, treat and monitor people with sleeping and respiratory disorders, such as obstructive sleep apnea (OSA). From time to time, for regulatory, quality, and marketing purposes, there may be a need to test the various products performance against PSG (gold standard technology), and other products. The purpose of this study is: 1. Products performance against PSG 2. comparison against other products, and 3. Assessments of potential new technologies

Key Dates

First listed
Mar 20, 2026
Start date
Apr 30, 2026
Status verified
Mar 2026
Primary completion
Oct 31, 2026
Completion
Oct 31, 2026

Study Design

Enrollment
90 participants (estimated)

Arms

  • Arm: OSA
    Suspected of obstructive sleep apnea and about to undergo assessment

Primary Outcome Measure

Sensitivity [ Time Frame: Single night PSG ]

Central Contacts

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