N/A
Completed N=35
Simulated In-House Usability Study of Eclipse Continuous Positive Airway Pressure (CPAP) Device
Source: ClinicalTrials.gov NCT05570747 ↗Enrolled (actual)
35
Serious AEs
0.0%
Results posted
Nov 2025
Primary outcomePrimary: Time to Complete Each Setup — 72.9; 14.6 seconds
Summary
The study is designed to assess the usability of a novel CPAP human interface compared to a traditional nasal mask. Human subjects will interact with two different CPAP interfaces including a traditional CPAP mask and the 2nd generation DreamPort-Eclipse. Subjects will be requested to put on each of the different CPAP interface options a total of three times for a total of 6 trials. The order of device will be randomized.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Time to Complete Each Setup |
72.9; 14.6 | — |
| PRIMARY Number of Technical Issues That Occurred During the Trial |
6; 15 | — |
| PRIMARY Number of Times Subjects Needed Additional Instructions |
3.7; 0 | — |
Eligibility Criteria
Inclusion Criteria
- Male or female ≥18 years old who are impacted by obstructive sleep apnea and currently are familiar with a CPAP device.
Exclusion Criteria
- Diagnosis of any medical or behavioral conditions that would compromise subject safety.
- Under the age of 18: target for this current version of the platform is the adult population.
Data sourced from ClinicalTrials.gov (NCT05570747). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.