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

NAActive, not recruitingINTERVENTIONAL
Enrollment

127

Participants

Timeline

Start Date

May 31, 2015

Primary Completion Date

March 31, 2025

Study Completion Date

June 30, 2025

Conditions
Obstructive Sleep Apnea
Interventions
DEVICE

Inspire® UAS System

This is a single-arm study; all participants will be implanted with the Inspire® UAS System, which is a permanent, implantable therapy that consists of three implantable components: an IPG, a stimulation lead, and a sensing lead. In addition, the study subject receives a remote control to activate the therapy.

Trial Locations (14)

10021

Weill Cornell Medicine, New York

15219

University of Pittsburgh Medical Center, Pittsburgh

19104

University of Pennsylvania, Division of Sleep Medicine, Philadelphia

19107

Thomas Jefferson University and Hospital, Philadelphia

29425

Medical University of South Carolina, Charleston

33183

South Miami Hospital, Miami

33606

Tampa General Hospital, Tampa

35294

The University of Alabama at Birmingham Medical Center, Birmingham

40218

Kentucky Research Group, Louisville

44106

University Hospitals, Cleveland

44195

Cleveland Clinic Foundation, Cleveland

45219

The Christ Hospital, Cincinnati

66160

The University of Kansas Medical Center, Kansas City

90033

University of Southern California, Los Angeles

Sponsors
All Listed Sponsors
lead

Inspire Medical Systems, Inc.

INDUSTRY