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Exploration of Current and New Technologies for Accuracy of Diagnosing OSA | Clinical Trials | Clareo Health

NOT_YET_RECRUITING

Exploration of Current and New Technologies for Accuracy of Diagnosing OSA

NCT07485582•ResMed

Summary

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

Eligibility

Age

18 - No limit years

Sex

ALL

Healthy Volunteers

Inclusion Criteria

•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

Exclusion Criteria

•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, e.g. severe insomnia)
•Who are or may be pregnant
•Participants are 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.
•Shift workers who worked an overnight shift in the past 3 days
•Participant who are contraindicated to use the NightOwl sensor

Locations (7)

Peninsula Sleep Clinic

Sydney, New South Wales, Australia

Adelaide Institute for Sleep Health (FHMRI Sleep Health), Flinders University

Adelaide, South Australia, Australia

Flinders Health and Medical Research Institute

Adelaide, South Australia, Australia

Centre for Sleep Science, The University of Western Australia.

Perth, UWA, Australia

Box Hill Hospital

Box Hill, Victoria, Australia

Victorian Respiratory Support Service (VRSS)

Heidelberg, Victoria, Australia

School of Psychological Science

Perth, Australia

Key Dates

Start Date

April 1, 2026

Primary Completion Date

October 1, 2026

Completion Date

October 1, 2026

Last Updated

March 20, 2026

Enrollment

ESTIMATED participants

Conditions

Obstructive Sleep Apnea

Interventions

Device A

DEVICE

Device B

DEVICE

Device C

DEVICE

Device D

DEVICE

Device E

DEVICE

Screener A

DIAGNOSTIC_TEST

Contacts

Alison Wimms, PhD

CONTACT

02 8884 2203 Alison.Wimms@resmed.com.au

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: March 20, 2026Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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Exploration of Current and New Technologies for Accuracy of Diagnosing OSA

Inclusion Criteria

Exclusion Criteria

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Digital-supported Orofacial Myofunctional Therapy in OSA

Maridebart Cafraglutide Versus Placebo in Adult Participants With Obstructive Sleep Apnea on Positive Airway Pressure Therapy

A Cross-sectional Study Examining Adipose Tissue in Obstructive Sleep Apnea

Diaphragm Ultrasound İn Children With OSAS

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