EURO-STIM Registry

Inspire Medical Systems

Status: Enrolling

Conditions: Obstructive Sleep Apnea (OSA); Obstructive Sleep Apnea

Treatments: Device: Inspire UAS System

Study type: Observational

Funder types: Industry

Identifiers

NCT06971796

2023-004

Details and patient eligibility

About

The registry is to measure longitudinal outcomes and adherence of the Inspire System. The goal of the registry is to capture the life cycle of the patient's use of the Inspire System through routine clinical care visits. There are no required interventions or testing.

Enrollment: 1,000 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

Any patient implanted with or receiving an Inspire implant, who meets the following criteria, is eligible to participate in the registry:

1. Capable of giving informed consent, as required per institution
2. Willing to return for routine clinic visits as required for Inspire therapy management

Exclusion criteria

Any patient who meets any of the following criteria will not be eligible to participate in the registry:

1. Has a life expectancy of less than one year
2. Any reason the clinician deems patient is unfit for participation in the study