Trials / Completed
CompletedNCT03948152
A Study to Determine Preferences Towards Interface Products
A Study to Determine Clinician and Patient Preferences Towards Interface Products Recommended by the 3D Mask Advice Tool
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 310 (actual)
- Sponsor
- Philips Respironics · Industry
- Sex
- All
- Age
- 21 Years – 85 Years
- Healthy volunteers
- Not accepted
Summary
Enrolled Naïve participants will be randomized to one of two arms, the investigational or control arm. Once randomized the institutions will fit the participant with the procedures outlined in the protocol. Each participant will be required to trial the mask for a period of 90 days. Any Unscheduled Visits or Calls that occur during the participants 90 days documented.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Standard of Care | Participants will have a Positive Airway Pressure (PAP) mask chosen to wear for a period of 90 days as provided by the sites standard of care. |
| OTHER | Mask Advice Tool | Participants will have a Positive Airway Pressure (PAP) mask chosen to wear for a period of 90 days as provided by the mask advice tool. |
Timeline
- Start date
- 2019-04-18
- Primary completion
- 2020-02-07
- Completion
- 2020-02-07
- First posted
- 2019-05-13
- Last updated
- 2020-07-07
Locations
5 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT03948152. Inclusion in this directory is not an endorsement.