CPAP In-home Assessment USA
NCT02809859 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 139
Last updated 2019-03-05
Summary
The study is to evaluate the product reliability, therapy effectiveness and user feedback of a Continuous Positive Airway Pressure (CPAP) device in-home for up to 6 months.
Conditions
Interventions
- DEVICE
-
Fisher & Paykel Healthcare CPAP Device
Fisher \& Paykel Healthcare CPAP Device
Sponsors & Collaborators
-
Fisher and Paykel Healthcare
lead INDUSTRY
Principal Investigators
-
Matt Uhles · Clayton Sleep Institute
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 22 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2016-07-31
- Primary Completion
- 2017-04-30
- Completion
- 2017-04-30
Countries
- United States
Study Locations
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