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RECRUITING
NCT07132307
NA

Reducing Obstructive Sleep Apnea After Hypoglossal Nerve Stimulation Through Mandibular Advancement

Sponsor: Washington University School of Medicine

View on ClinicalTrials.gov

Summary

The purpose of this study is to evaluate the effectiveness, feasibility, and safety of mandibular advancement devices (MAD) for treating severe obstructive sleep apnea (OSA) in patients who are CPAP intolerant and have failed hypoglossal nerve stimulation (HGNS).

Official title: Reducing Obstructive Sleep Apnea After Hypoglossal Nerve Stimulation Through

Key Details

Gender

All

Age Range

18 Years - 70 Years

Study Type

INTERVENTIONAL

Enrollment

30

Start Date

2025-07-29

Completion Date

2027-02-01

Last Updated

2026-03-19

Healthy Volunteers

No

Interventions

DEVICE

Mandibular advancement device (MAD)

The intervention in this study involves fitting and using a mandibular advancement device (MAD), specifically the ProSomnus Sleep Device, to treat moderate to severe obstructive sleep apnea (OSA) in patients who are intolerant to CPAP and have failed hypoglossal nerve stimulation (HGNS) therapy.

Locations (1)

Washington University School of Medicine

St Louis, Missouri, United States