[{"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":41,"hasResults":42,"nctId":43,"briefTitle":44,"officialTitle":45,"acronym":31,"eligibilityCriteria":46,"healthyVolunteers":42,"sex":47,"minAge":48,"maxAge":49,"enrollmentInfo":50,"targetDuration":31,"studyType":53,"phases":54,"briefSummary":56,"conditions":57,"keywords":60,"overallStatus":64,"whyStopped":31,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"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","tonsillectomy-vs-tonsillotomy-in-adults-with-obstructive-sleep-apnea-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":51,"type":52},464,"ESTIMATED","INTERVENTIONAL",[55],"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.",[58,59],"Obstructive Sleep Apnea","Tonsillar Hypertrophy",[9,61,15,62,63],"Obstructive sleep apnea (OSA)","Intracapsular reduction of tonsils","Drug Induced Sedation Endoscopy","NOT_YET_RECRUITING","2024-04-18",{"date":67,"type":68},"2024-04-19","ACTUAL",{"date":70,"type":52},"2025-01",{"date":72,"type":52},"2027-09",{"name":5,"class":6}]