[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100545014":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":31,"centralContacts":32,"locations":31,"responsibleParty":38,"collaborators":31,"id":40,"slug":31,"hasResults":41,"nctId":42,"briefTitle":43,"officialTitle":44,"acronym":31,"eligibilityCriteria":45,"healthyVolunteers":41,"sex":46,"minAge":47,"maxAge":48,"enrollmentInfo":49,"targetDuration":31,"studyType":52,"phases":53,"briefSummary":55,"conditions":56,"keywords":59,"overallStatus":63,"whyStopped":31,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":31},{"fullName":5,"class":6},"University of Aarhus","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Tonsillectomy","ACTIVE_COMPARATOR","Patients undergo standard removal of subcapsular removal of palatine tonsils",[13],"Procedure: Tonsillectomy",{"label":15,"type":16,"description":17,"interventionNames":18},"Tonsillotomy","EXPERIMENTAL","Patients undergo intracapsular reduction of palatine tonsils",[19],"Procedure: Tonsillotomy",[21,27],{"type":22,"name":9,"description":23,"armGroupLabels":24,"otherNames":25},"PROCEDURE","Standard tonsillectomy",[9],[26],"TE",{"type":22,"name":15,"description":15,"armGroupLabels":28,"otherNames":29},[15],[30],"TT",null,[33],{"name":34,"role":35,"phone":36,"phoneExt":31,"email":37},"Kasra Zainali-Gill, Ph.D","CONTACT","+4578439744","kasrzain@rm.dk",{"type":39,"investigatorFullName":31,"investigatorTitle":31,"investigatorAffiliation":31,"oldNameTitle":31,"oldOrganization":31},"SPONSOR","100545014",false,"NCT06376383","Tonsillectomy vs. Tonsillotomy in Adults With Obstructive Sleep Apnea","Tonsillectomy Versus Tonsillotomy in Adults With Obstructive Sleep Apnea; a Randomized Controlled Trial Comparing Postoperative Morbidity","Inclusion Criteria:\n\n* Age \\> 18 years\n* Tonsil size 2, 3, or 4 (Friedman tonsil scale)\n* Confirmed OSA with sleep analysis not older than a year either CRM or PSG\n* ASA 1 or 2\n* BMI \\\u003C 35 kg\u002Fm2\n\nExclusion Criteria:\n\nChildren age \\\u003C 18 years\n\n* Previous pharyngeal surgery such as previous tonsillotomy, tonsillectomy or palatal surgery\n* Epileptic disease or severe neurological comorbidity.\n* ASA 3, or 4.\n* Central sleep apnea\n* Previous thrombotic disease.\n* Currently treated with sleep medications\n* No collapse of oropharyngeal lateral wall during DISE\n* Dropout of study, lack of sleep analysis or lack of postoperative DISE.","ALL","18 Years","65 Years",{"count":50,"type":51},464,"ESTIMATED","INTERVENTIONAL",[54],"NA","The primary purpose of this randomized controlled trial s to investigate whether surgical reduction of palatine tonsils (tonsillotomy) is a superior treatment compared to complete surgical removal of palatine tonsils (tonsillectomy) in adults patients with obstructive sleep apnea and concomitant enlarged tonsils in regards of perioperative and postoperative morbidity.",[57,58],"Obstructive Sleep Apnea","Tonsillar Hypertrophy",[9,60,15,61,62],"Obstructive sleep apnea (OSA)","Intracapsular reduction of tonsils","Drug Induced Sedation Endoscopy","NOT_YET_RECRUITING","2024-04-18",{"date":66,"type":67},"2024-04-19","ACTUAL",{"date":69,"type":51},"2025-01",{"date":71,"type":51},"2027-09",{"name":5,"class":6}]