[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100561139":3},{"organization":4,"armGroups":7,"interventions":10,"overallOfficials":12,"centralContacts":17,"locations":28,"responsibleParty":64,"collaborators":66,"id":69,"slug":10,"hasResults":70,"nctId":71,"briefTitle":72,"officialTitle":73,"acronym":74,"eligibilityCriteria":75,"healthyVolunteers":70,"sex":76,"minAge":77,"maxAge":10,"enrollmentInfo":78,"targetDuration":81,"studyType":82,"phases":10,"briefSummary":83,"conditions":84,"keywords":87,"overallStatus":31,"whyStopped":10,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":101,"completionDateStruct":103,"leadSponsor":105,"locationsCount":106},{"fullName":5,"class":6},"Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":10},"Patients scheduled for elective surgery with a diagnosis of obstructive sleep apnea (OSA)",null,"* Patients scheduled for elective surgery at the operating theatres of the AUMC with a diagnosis of OSA with or without treatment\n* Patients with continuous positive airway pressure (CPAP) or mandibular advancement device (MAD) are considered patients with treatment for OSA\n* Patients ≥ 18 years\n* Dutch or English speaking\n* Willing and able to sign consent for re-use of care data",[13],{"name":14,"affiliation":15,"role":16},"Jeroen Hermanides, Prof. Dr.","AmsterdamUMC","PRINCIPAL_INVESTIGATOR",[18,24],{"name":19,"role":20,"phone":21,"phoneExt":22,"email":23},"Martin V.H. Rutten, Msc, MD","CONTACT","+31205669111","28657","m.v.rutten@amsterdamumc.nl",{"name":14,"role":20,"phone":25,"phoneExt":26,"email":27},"+310205669111","62533","j.hermanides@amsterdamumc.nl",[29,49],{"facility":30,"status":31,"city":32,"state":33,"zip":34,"country":35,"cosmosGeoPoint":36,"geoPoint":41,"contacts":42},"AmsterdamUMC, location AMC","RECRUITING","Amsterdam","North Holland","1105 AZ","Netherlands",{"type":37,"coordinates":38},"Point",[39,40],4.88969,52.37403,{"lat":40,"lon":39},[43,46,48],{"name":44,"role":20,"phone":45,"phoneExt":22,"email":23},"Martin Rutten, Msc, MD","+31(0)205669111",{"name":44,"role":20,"phone":47,"phoneExt":10,"email":23},"+31 (0)653326924",{"name":44,"role":16,"phone":10,"phoneExt":10,"email":10},{"facility":50,"status":31,"city":32,"state":10,"zip":51,"country":35,"cosmosGeoPoint":52,"geoPoint":54,"contacts":55},"Amsterdam UMC location VuMC","1081 HV",{"type":37,"coordinates":53},[39,40],{"lat":40,"lon":39},[56,59,63],{"name":57,"role":20,"phone":58,"phoneExt":10,"email":23},"Martin Rutten","+31 6 50075296",{"name":60,"role":20,"phone":61,"phoneExt":22,"email":62},"Luca den Tenter","+31 205669111","l.m.dententer@amsterdamumc.nl",{"name":57,"role":16,"phone":10,"phoneExt":10,"email":10},{"type":16,"investigatorFullName":57,"investigatorTitle":65,"investigatorAffiliation":5,"oldNameTitle":10,"oldOrganization":10},"MSc, MD",[67],{"name":68,"class":6},"VU University of Amsterdam","100561139",false,"NCT06586268","The SNORE-trial: Analysis of Alterations in Sleep Stages Following Anesthesia and Their Relation to the Severity of Obstructive Sleep Apnea in the First 3 Nights After Surgery","The SNORE-trial: Postoperative REM-Sleep Disturbance iN Obstructive Sleep-apnea Patients and the Relation With AH-index","SNORE","Inclusion Criteria:\n\n* Patients scheduled for elective surgery at the operating theatres of the AUMC with a diagnosis of OSA with or without treatment with an expected admittance of a minimum of 3 days\n* Patients with continuous positive airway pressure (CPAP) or mandibular advancement device (MAD) are considered patients with treatment for OSA\n* Patients ≥ 18 years\n* Dutch or English speaking\n* Willing and able to sign consent for re-use of care data\n\nExclusion Criteria:\n\n* Patients \\< 18 years\n* Not speaking Dutch or English\n* Patients who do not sign consent for re-use of care data\n* Surgery scheduled in day case or with an expected discharge before the third night after surgery","ALL","18 Years",{"count":79,"type":80},35,"ESTIMATED","3 Days","OBSERVATIONAL","The goal of this observational study is to learn about the relationship between sleep alterations following anesthesia and their relationship to a potential increase of obstructive sleep apnea (OSA) severity.\n\nOur main question is: Is there an increased severity of OSA on the third post-operative night compared to the first post-operative night and does this have a relation with REM sleep?\n\nParticipants enrolled in this research are all diagnosed with OSA, with or without treament. All participants will be asked to wear a watchlike device called WATCHPAT to identify sleep paterns and register apneic (no breathing) and hypopneic (insufficient breathing) incidents. We ask our participants to wear this device for 8-10 hours a night when they are a sleep.",[85,86],"Sleep Apnea Syndrome, Obstructive","Sleep Apnea Syndrome (OSAS)",[88,89,90,91,92,93,94,95,96],"OSAS","OSA","obstructive sleep apnea","Post-surgical","post-anesthesia","REM sleep","PACU","AHI","Desaturations","2025-01-28",{"date":99,"type":100},"2025-01-29","ACTUAL",{"date":102,"type":100},"2024-10-01",{"date":104,"type":80},"2025-08",{"name":5,"class":6},2]