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Study identifier: NCT07186725 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Home-based Under Mattress Monitor for OSA

Condition: Obstructive Sleep Apnea (OSAS) · Obstructive Sleep Apnea (SAOS)  ·  Sponsor: Isabel Moreno Hay

PhaseNA
Planned participants70
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNo

About this study

The aim of the study is to evaluate the effectiveness of the under-mattress monitoring device to aid in the titration process of a mandibular advancement device (MAD) for the management of obstructive sleep apnea (OSA). A secondary aim is to evaluate changes in subjective OSA symptoms and patient's satisfaction with MAD. A third aim is to analyze if there are differences between the sleep parameters recorded by the under-mattress monitor between responders and non-responders to MAD therapy.

This description comes directly from the study's public registry record.

Talk to the study team

Sumia Alyousef, BDS  ·  (859) 323-3440  ·  Sumia.Alyousef@uky.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of KentuckyLexington, Kentucky, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07186725