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Clinical Trial Summary

The main purpose of this study is to test is mandibular advacenment device (MAD) use is associated with reductions in nocturia.


Clinical Trial Description

After been informed about the study and informed about risks and benefits, participants will be fitted with a MAD and will be asked to completed questionnaires at baseline, in between follow ups and during follow ups. Nocturia will be assess and appliance will be titrated every 2 weeks until participants report less than 2 voiding per night according to the daily dairies. At that point, second sleep study with MAD in place will be performed to assess treatment effectiveness. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05562388
Study type Interventional
Source University of Kentucky
Contact Fernanda Yanez Regonesi, DDS, MS
Phone 8593235500
Email fya232@uky.edu
Status Recruiting
Phase N/A
Start date July 31, 2023
Completion date August 1, 2024

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