[{"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":24},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,38],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":17,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":4,"overallStatus":25,"whyStopped":4,"lastUpdateSubmitDate":26,"lastUpdatePostDateStruct":27,"startDateStruct":30,"completionDateStruct":32,"leadSponsor":34,"locationsCount":37},"100640011","fasting-time-and-post-tonsillectomy-pain-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":19,"type":20},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.",[24],"Tonsillar Disorder","NOT_YET_RECRUITING","2026-05-05",{"date":28,"type":29},"2026-05-08","ACTUAL",{"date":31,"type":20},"2026-06",{"date":33,"type":20},"2029-05",{"name":35,"class":36},"Brittany Willer","OTHER",1,{"id":39,"slug":40,"hasResults":11,"nctId":41,"briefTitle":42,"officialTitle":43,"acronym":44,"eligibilityCriteria":45,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":46,"targetDuration":4,"studyType":48,"phases":49,"briefSummary":51,"conditions":52,"keywords":4,"overallStatus":53,"whyStopped":4,"lastUpdateSubmitDate":54,"lastUpdatePostDateStruct":55,"startDateStruct":57,"completionDateStruct":59,"leadSponsor":61,"locationsCount":37},"100427988","modality-of-pain-management-in-ambulatory-tonsillectomy-surgery-in-adults-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":47,"type":20},30,"INTERVENTIONAL",[50],"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.",[24],"RECRUITING","2024-09-05",{"date":56,"type":29},"2024-09-19",{"date":58,"type":29},"2021-06-09",{"date":60,"type":20},"2024-12-31",{"name":62,"class":36},"Centre Hospitalier Universitaire de Besancon"]