[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"obstructive-sleep-apnea-saos\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:obstructive-sleep-apnea-saos":47},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":10,"sex":15,"minAge":16,"maxAge":17,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":28,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":5},"100607297",false,"NCT07186725","Home-based Under Mattress Monitor for OSA","Home-Based Under-Mattress Monitoring Device to Estimate Mandibular Advancement in Oral Appliance Therapy for Obstructive Sleep Apnea","Inclusion Criteria:\n\n* Diagnosis of Obstructive Sleep Apnea demonstrated with a sleep study polysomnography or home sleep study (PSG or HSAT), manually scored by a sleep physician according to the 2017 American Academy of Sleep medicine scoring guidelines.\n* Willingness to commute to the OFP clinic every 2 weeks during MAD titration period.\n* Consent to partake in the study.\n\nExclusion Criteria:\n\n* Diagnosis of central or mixed sleep apnea.\n* Neurocognitive disease.\n* Concomitant therapy with PAP therapy.\n* Allergic to the appliance material (Polyamide 12).\n* Presence of active dental decay, ill-fitting dental restorations, or crown to root ratio unfavorable.\n* Inadequate English language comprehension.\n* Lack of coordination or dexterity to insert\u002Fremove the MAD intraorally.\n* Inability to tolerate digital dental impressions.\n* Patients with concomitant diagnosed sleep disorders, including narcolepsy, restless leg syndrome, rapid eye movement sleep behavior disorder).","ALL","18 Years","80 Years",{"count":19,"type":20},70,"ESTIMATED","INTERVENTIONAL",[23],"NA","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.",[26,27],"Obstructive Sleep Apnea (OSAS)","Obstructive Sleep Apnea (SAOS)",[29,30,31,32,33,34],"Mandibular Advancement","Sleep Apnea","Oral Appliance","Home-based","Obstructive Sleep Apnea","Home-based device","RECRUITING","2026-02-02",{"date":38,"type":39},"2026-02-03","ACTUAL",{"date":41,"type":39},"2026-01-07",{"date":43,"type":20},"2027-03",{"name":45,"class":46},"Isabel Moreno Hay","OTHER",""]