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Inspire® Post-Approval Study / Protocol Number 2014-001

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NCT02413970

Sponsored by Inspire Medical Systems, Inc. (industry) · INSP — their whole pipeline →.

Phase
Not applicable
Status
Unknown status
Study type
Interventional
Design
Na · None · Treatment
Enrollment
127actual
Sites
14
Country
United States

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 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
StartMay 2015actualWhen the study began enrolling
Primary completionMar 2025estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionJun 2025estimatedThe whole study's end, after follow-up
First posted2015-04-10estimatedWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2024-12-27actualThe 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: Inspire® UAS System — also filed as Inspire® therapy

Primary outcomes

what the primary-completion date above is the date OF
Long-term Device-Related SAEs
measured 5 Years Post-Implant
Therapy Specific AEs
measured 12 Months Post-Implant
Long-term Therapy-Related AEs
measured 5 Years Post-Implant

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