EURO-STIM Registry

Launched by INSPIRE MEDICAL SYSTEMS, INC. · May 7, 2025

Keywords

ClinConnect Summary

The EURO-STIM Registry is a study designed to track how well the Inspire System works for people with Obstructive Sleep Apnea (OSA) over time. The Inspire System is a device that helps patients breathe better while they sleep. This registry will collect information during regular doctor visits to see how patients are doing with their treatment. Importantly, there are no special tests or treatments required for participants in this study.

To participate, patients must have the Inspire implant and be able to give their consent. They should also be willing to come back for routine check-ups to help manage their therapy. However, individuals with a life expectancy of less than one year or those deemed unfit by their doctor cannot join. The registry is not yet recruiting participants, but it aims to include all eligible patients, regardless of gender, aged 65 and older. This study will provide valuable insights into the long-term effectiveness and use of the Inspire System for treating OSA.

Gender

ALL

Eligibility criteria

• 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