PAP Systems External Clinical Studies (ECS)
← catalyst calendarNCT06562205 · readout in 774 d
Sponsored by ResMed (industry) · RMD — their whole pipeline →.
Phase
Not applicable
Status
Not yet recruiting
Study type
Interventional
Design
Randomized · Single · Treatment
Enrollment
30estimated
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| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2028-08-01 | estimated | When the study began enrolling |
| Primary completion | 2028-10-01 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2028-10-29 | estimated | The whole study's end, after follow-up |
| First posted | 2024-08-20 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-04-24 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Obstructive Sleep Apnea
Interventions
- Device: PAP System A (with Amalfi) then PAP System B (with CLA11)
- Device: PAP System B (with CLA11) then PAP System A (with Amalfi)
Primary outcomes
what the primary-completion date above is the date OF(usability) Comparison of the usability of an investigational component/s of the PAP system to a comparison component/s of the PAP system and/or Criterion Score of 6
measured 6 weeks
(efficacy) Comparison of the investigational component/s of the PAP system efficacy (AHI) to a comparison component/s of the PAP system and/or clinically relevant data
measured 6 weeks
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