[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"tonsillar-disorder\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:tonsillar-disorder":61},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,37],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":10,"sex":15,"minAge":4,"maxAge":16,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":4,"briefSummary":21,"conditions":22,"keywords":4,"overallStatus":24,"whyStopped":4,"lastUpdateSubmitDate":25,"lastUpdatePostDateStruct":26,"startDateStruct":29,"completionDateStruct":31,"leadSponsor":33,"locationsCount":36},"100640011",false,"NCT07574476","Fasting Time and Post-tonsillectomy Pain","Fasting Duration and Post-tonsillectomy Pain in Pediatric Patients","Inclusion Criteria:\n\n* undergoing elective tonsillectomy with or without adenoidectomy and\u002For tympanostomy tube placement\n\nExclusion Criteria:\n\n* non-elective or urgent procedures\n* inpatient admission prior to surgery; patients with any missing required data\n* patients with conditions requiring deviation from standard anesthetic management (as determined by the anesthesiologist)","ALL","18 Years",{"count":18,"type":19},350,"ESTIMATED","OBSERVATIONAL","This is a prospective, observational study to determine the association between preoperative fasting duration and post-tonsillectomy pain scores in the post-anesthesia care unit (PACU) among pediatric patients undergoing tonsillectomy with or without adenoidectomy and\u002For tympanostomy tube placement. The primary outcome is the post-tonsillectomy pain score, with the secondary outcomes as total postoperative opioid consumption, PACU length of stay, and hospital length of stay.",[23],"Tonsillar Disorder","NOT_YET_RECRUITING","2026-05-05",{"date":27,"type":28},"2026-05-08","ACTUAL",{"date":30,"type":19},"2026-06",{"date":32,"type":19},"2029-05",{"name":34,"class":35},"Brittany Willer","OTHER",1,{"id":38,"slug":4,"hasResults":10,"nctId":39,"briefTitle":40,"officialTitle":41,"acronym":42,"eligibilityCriteria":43,"healthyVolunteers":10,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":44,"targetDuration":4,"studyType":46,"phases":47,"briefSummary":49,"conditions":50,"keywords":4,"overallStatus":51,"whyStopped":4,"lastUpdateSubmitDate":52,"lastUpdatePostDateStruct":53,"startDateStruct":55,"completionDateStruct":57,"leadSponsor":59,"locationsCount":36},"100427988","NCT04853173","Modality of Pain Management in Ambulatory Tonsillectomy Surgery in Adults","Modality of Pain Management in Ambulatory Tonsillectomy Surgery in Adults: External Pilot Study","DACAA","Inclusion Criteria:\n\n* programmed Tonsillectomy surgery\n\nExclusion Criteria:\n\n* Congenital or acquired hemostasis disorder\n* Indication of uvulo-bike-pharyngo-plasty\n* Contraindication to the use of one of the protocol molecules including pregnancy\n* Allergy to analgesic treatments used in the study\n* Ongoing analgesic treatment that cannot be interrupted",{"count":45,"type":19},30,"INTERVENTIONAL",[48],"NA","No SFORL recommendation for adult ambulatory tonsillectomy. This study would allow the establishment of an ambulatory management during an adult tonsillectomy. This would allow a return home from J0 for the patient and therefore would improve the comfort of the patients and reduce the cost associated with a conventional hospitalization over several days.",[23],"RECRUITING","2024-09-05",{"date":54,"type":28},"2024-09-19",{"date":56,"type":28},"2021-06-09",{"date":58,"type":19},"2024-12-31",{"name":60,"class":35},"Centre Hospitalier Universitaire de Besancon",""]