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Post Market Clinical Follow up of ResMed Mask Systems

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NCT05262439 · readout ≤ 315 d

Sponsored by ResMed (industry) · RMD — their whole pipeline →.

Phase
Not applicable
Status
Recruiting
Study type
Interventional
Design
Na · None · Treatment
Enrollment
500estimated
Sites
1
Country
Australia

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2022-05-26actualWhen the study began enrolling
Primary completionJun 2027estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionJun 2027estimatedThe whole study's end, after follow-up
First posted2022-03-02actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-04-29actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Obstructive Sleep Apnea

Intervention

  • Device: New generation CPAP mask

Primary outcomes

what the primary-completion date above is the date OF
Apnea Hypopnea Index (event/hour)
measured up to 90 days
Usage Hours (hours/night)
measured up to 90 days
Leak (L/minute)
measured up to 90 days
CPAP Pressure (cmH2O)
measured up to 90 days
Adverse Events
measured up to 90 days

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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