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CompletedNCT02809859

CPAP In-home Assessment USA

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
139 (actual)
Sponsor
Fisher and Paykel Healthcare · Industry
Sex
All
Age
22 Years
Healthy volunteers
Not accepted

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.

Detailed description

Existing and Naïve CPAP users will be recruited into a 6 month in-home study Participants will attend 5 study visits at day 0, 7, 30, 60 and 180. Outcome of the clinical investigation include downloadable device data reports, device error reports and participants perception questionnaires.

Conditions

Interventions

TypeNameDescription
DEVICEFisher & Paykel Healthcare CPAP DeviceFisher \& Paykel Healthcare CPAP Device

Timeline

Start date
2016-07-01
Primary completion
2017-04-01
Completion
2017-04-01
First posted
2016-06-22
Last updated
2019-03-05
Results posted
2019-03-05

Locations

4 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT02809859. Inclusion in this directory is not an endorsement.

CPAP In-home Assessment USA (NCT02809859) · Clinical Trials Directory