PAP-NAP Device Clinical Study
← catalyst calendarNCT07785310 · readout in 371 d
Sponsored by ResMed (industry) · RMD — their whole pipeline →.
Phase
Not applicable
Status
Not yet recruiting
Study type
Interventional
Design
Na · None · Other
Enrollment
10estimated
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 2026-08-25
Dates
each axis at the precision it was filed, with the registry's own basis| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2027-01-01 | estimated | When the study began enrolling |
| Primary completion | 2027-09-01 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2027-09-01 | estimated | The whole study's end, after follow-up |
| First posted | 2026-08-25 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-08-25 | 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
Intervention
- Device: APL Device
Primary outcome
what the primary-completion date above is the date OFFeasibility and Usability of the Investigational APL PAP Device During a Supervised Daytime PAP-NAP Session
measured Immediately following the supervised daytime nap session (single study visit; up to 3 hours)
Related
RMD · their whole pipeline · Obstructive Sleep Apnea readouts · Congress trades in RMD · Executive-branch trades in RMD
RMD's other studiesmost recently updated first
- Exploration of Current and New Technologies for Accuracy of Diagnosing OSA — · Not yet recruiting
- Long-term Observation of PAP-therapy With Telemonitoring: Telemedicine Registry TelePAP — · Completed
- HomeVent ( Connect) Registry: EU COPD Home NIV Registry — · Completed
- Registry Study on Prescription, Patient Pathways, Therapy Efficacy and Usage of Mandibular Advancement Devices in Obstructive Sleep Apnea - PATT-OSA Registry — · Active, not recruiting
- Data Collection Study to Review Novel Methods for Diagnosing Obstructive Sleep Apnea — · Recruiting
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