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Home-based Under Mattress Monitor for OSA

StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Lead sponsor: [Redacted] to Isabel Moreno Hayv4 Show 5 more changesShow less
    • Trial status: Withheld to Recruiting
    • Primary and study completion dates: Mar 2027
    • Start date: Jan 7, 2026
    • Collaborators expanded, about 6 words
    • Study title shortened, about 7 words
  2. 2 versions Re-verified since Nov 14, 2025, no change to tracked fieldsv2-v3
  3. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT07186725
Lead Sponsor Isabel Moreno Hay
Collaborators: American Academy of Dental Sleep Medicine
Conditions
(from sponsor)		 Obstructive Sleep Apnea (OSAS), Obstructive Sleep Apnea (SAOS)
Related terms Sleep Apnea Syndromes, Sleep Apnea, Obstructive
Enrollment 70 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov