Clinical Trial

Myofunctional Therapy for Obstructive Sleep Apnea

Enrolling by Invitation
View on ClinicalTrials.gov →
Summary
The purpose of this study is to explore a new way to examine the function of the muscles using a technique called high-resolution manometry. The study will enroll 30 adults with OSA, all of whom will use the myofunctional therapy (MFT) devices for 3 months. High-resolution manometry will be used to measure the amount of pressure generated by the muscles of the throat when drinking water or breathing air, both with and without the MFT devices, and before and after the MFT intervention. If successful, this method can help us understand why sleep improves after MFT.
Protocol Amendment History 3 changes
critical Trial status changed: Recruiting → Enrolling by Invitation 2026-07-31
critical Trial status changed: Enrolling by Invitation → Recruiting 2026-06-19
critical Trial status changed: Not Yet Recruiting → Enrolling by Invitation 2026-04-17
Trial Details
NCT Number NCT07301125
Lead Sponsor University of Minnesota
Conditions Obstructive Sleep Apnea
Enrollment 30 participants
Start Date 2026-08-17
Primary Completion 2027-09-30 (estimated)
Study Completion 2027-09-30 (estimated)
Updated on ClinicalTrials.gov 2026-07-30