[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100377206":3},{"organization":4,"outcomesModule":7,"designInfo":17,"detailedDescription":11,"studyPopulation":20,"armGroups":21,"interventions":11,"overallOfficials":11,"centralContacts":26,"locations":32,"responsibleParty":53,"collaborators":11,"id":55,"slug":56,"hasResults":57,"nctId":58,"briefTitle":59,"officialTitle":59,"acronym":11,"eligibilityCriteria":60,"healthyVolunteers":57,"sex":61,"minAge":62,"maxAge":11,"enrollmentInfo":63,"targetDuration":11,"studyType":66,"phases":11,"briefSummary":67,"conditions":68,"keywords":70,"overallStatus":35,"whyStopped":11,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":76,"completionDateStruct":78,"leadSponsor":80,"locationsCount":81},{"fullName":5,"class":6},"Thomas Jefferson University","OTHER",{"primaryOutcomes":8,"secondaryOutcomes":11,"otherOutcomes":11},[9,13,15],{"measure":10,"description":11,"timeFrame":12},"Difference in polysomnography (PSG) data between UAS and CPAP groups",null,"2 years",{"measure":14,"description":11,"timeFrame":12},"Difference in Epworth Sleepiness Scale questionnaire data between UAS and CPAP groups",{"measure":16,"description":11,"timeFrame":12},"Difference in Functional Outcomes of Sleep questionnaire data between UAS and CPAP groups",{"allocation":11,"interventionModel":11,"interventionModelDescription":11,"primaryPurpose":11,"observationalModel":18,"timePerspective":19,"maskingInfo":11},"COHORT","PROSPECTIVE","Patients using upper airway stimulation or continuous positive airway pressure",[22,24],{"label":23,"type":11,"description":11,"interventionNames":11},"Upper airway stimulation",{"label":25,"type":11,"description":11,"interventionNames":11},"Continuous positive airway pressure",[27],{"name":28,"role":29,"phone":30,"phoneExt":11,"email":31},"Beth Duddy, RN","CONTACT","215-955-9880","elizabeth.duddy@jefferson.edu",[33],{"facility":34,"status":35,"city":36,"state":37,"zip":38,"country":39,"countryCode":40,"cosmosGeoPoint":41,"geoPoint":46,"contacts":47},"Thomas Jefferson University Department of Otolaryngology","RECRUITING","Philadelphia","Pennsylvania","19107","United States","US",{"type":42,"coordinates":43},"Point",[44,45],-75.16362,39.95238,{"lat":45,"lon":44},[48,50],{"name":49,"role":29,"phone":11,"phoneExt":11,"email":11},"Elizabeth Duddy, RN, BSN",{"name":51,"role":52,"phone":11,"phoneExt":11,"email":11},"Colin Huntley, MD","PRINCIPAL_INVESTIGATOR",{"type":54,"investigatorFullName":11,"investigatorTitle":11,"investigatorAffiliation":11,"oldNameTitle":11,"oldOrganization":11},"SPONSOR","100377206","head-to-head-comparison-of-upper-airway-stimulation-and-continuous-positive-airway-pressure-a-pilot-study-100377206",false,"NCT04191512","Head to Head Comparison of Upper Airway Stimulation and Continuous Positive Airway Pressure; a Pilot Study.","Inclusion Criteria:\n\n* Age greater than 22 years old\n* History of moderate to severe OSA (AHI 15-65)\n* UAS implantation with postoperative titration and demonstrated successful use of therapy or has demonstrated the ability to tolerate CPAP for greater than 4 hours per night 5 days per week.\n\nExclusion Criteria:\n\n* none","ALL","22 Years",{"count":64,"type":65},50,"ESTIMATED","OBSERVATIONAL","To date, there has been no head to head comparison of Upper Airway Stimulation (UAS) and Continuous Positive Airway Pressure (CPAP) utilizing a full night polysomnographic evaluation. With this study we aim to evaluate a pilot cohort of patients with OSA treated with CPAP or UAS using the WatchPAT polysomnography system.",[69],"Obstructive Sleep Apnea",[69,71],"Continuous Positive Airway Pressure","2026-09-28",{"date":74,"type":75},"2026-09-29","ACTUAL",{"date":77,"type":75},"2019-11-19",{"date":79,"type":65},"2027-06-30",{"name":5,"class":6},1]