[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"adenoidectomy\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:adenoidectomy":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,46,70],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":29,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100643818","coblator-wand-comparative-analysis-100643818",false,"NCT07635719","Coblator Wand Comparative Analysis","Comparative Analysis of Efficiency, Technical Performance, and Environmental Cost Between Reprocessed and New Coblator Wands in Intracapsular Tonsillectomies and Adenoidectomies","Inclusion Criteria:\n\n* Pediatric patients scheduled for tonsillectomy and\u002For adenoidectomy\n* Parental consent and child assent (when applicable)\n\nExclusion Criteria:\n\n* Pregnancy","ALL","1 Year","18 Years",{"count":20,"type":21},30,"ESTIMATED","INTERVENTIONAL",[24],"NA","This study will address the gap in coblator wands by comparing the performance of reprocessed coblator wands with new wands in terms of efficiency and technical issues. As part of the evaluation, the investigator team will conduct the technical performance of the life cycle assessment of reprocessed versus new coblation wands based on the methodology described in the literature (see References) in studies of laryngoscopes.",[27,28],"Tonsillectomy","Adenoidectomy",[30,31,32],"Coblator wand","Product performance","Usability","NOT_YET_RECRUITING","2026-06-03",{"date":36,"type":37},"2026-06-09","ACTUAL",{"date":39,"type":21},"2026-06",{"date":41,"type":21},"2026-12",{"name":43,"class":44},"Montefiore Medical Center","OTHER",1,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":11,"sex":16,"minAge":53,"maxAge":54,"enrollmentInfo":55,"targetDuration":4,"studyType":22,"phases":57,"briefSummary":58,"conditions":59,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":64,"completionDateStruct":66,"leadSponsor":68,"locationsCount":45},"100633482","effects-of-adenoidectomy-on-symptoms-and-ige-levels-in-children-with-ar-100633482","NCT07527260","Effects of Adenoidectomy on Symptoms and IgE Levels in Children With AR","Effects of Adenoidectomy With or Without Tonsillectomy on Symptoms and Local IgE Levels in Children With Allergic Rhinitis","Inclusion Criteria:\n\n\\- 3-12 years\n\n1. Children with physician-diagnosed allergic rhinitis and typical symptoms (nasal obstruction, watery rhinorrhea, paroxysmal sneezing);\n2. Co-existing adenoidal and tonsillar hypertrophy meeting surgical indications;\n3. No systemic or topical corticosteroids, leukotriene antagonists, or antihistamines within the past 3 months.\n\nExclusion Criteria:\n\n1. Prior adenoidectomy, tonsillectomy, or radio-frequency ablation;\n2. Nasal polyps, cystic fibrosis, primary ciliary dyskinesia, fungal rhinosinusitis, systemic vasculitis\u002Fgranulomatosis, tumor, or immunodeficiency;\n3. Endoscopic nasal surgery within 6 months or severe asthma precluding surgery;\n4. Upper respiratory infection within 4 weeks;\n5. Serious metabolic, cardiovascular, immune, neurologic, hematologic, gastrointestinal, cerebrovascular, or respiratory disease, or any condition judged by the investigator to interfere with outcome assessment or participant safety;\n6. Currently enrolled or within 30 days of participation in another clinical trial.","3 Years","12 Years",{"count":56,"type":21},36,[24],"This study aims to evaluate the effects of conservative management versus surgical intervention (adenoidectomy alone or adenotonsillectomy) on symptoms and local IgE levels in children with allergic rhinitis (AR) accompanied with adenotonsillar hypertrophy. The primary objectives include the impact of conservative management and surgical interventions on AR symptoms and local IgE levels. The second outcomes include serum IgE levels, inflammatory cell profiles within the nasal mucosa, and postoperative complications.",[28,27,60],"Allergic Rhinitis","2026-04-13",{"date":63,"type":37},"2026-04-14",{"date":65,"type":21},"2026-04-11",{"date":67,"type":21},"2027-04-01",{"name":69,"class":44},"Tongji Hospital",{"id":71,"slug":72,"hasResults":11,"nctId":73,"briefTitle":74,"officialTitle":75,"acronym":4,"eligibilityCriteria":76,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":77,"enrollmentInfo":78,"targetDuration":4,"studyType":22,"phases":80,"briefSummary":81,"conditions":82,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":85,"lastUpdatePostDateStruct":86,"startDateStruct":88,"completionDateStruct":90,"leadSponsor":92,"locationsCount":45},"100601263","lateral-positioning-for-extubation-after-adenotonsillectomy-100601263","NCT07108218","Lateral Positioning for Extubation After Adenotonsillectomy","Lateral Positioning During the Anesthesia Emergence After Ambulatory Adenotonsillectomy in Children on Postoperative Respiratory Adverse Events: a Multi-center Randomized Controlled Trial","Inclusion criteria:\n\n1. Subjects aged 1-6 years old without gender limit.\n2. Scheduled for an ambulatory adenotonsillectomy under general anesthesia.\n3. American Society of Anesthesiologists (ASA) classification grade I or II.\n4. Informed consent obtained from the patients' parents or legal guardians, who have expressed willingness to cooperate.\n\nExclusion criteria:\n\n1. Presence of concomitant cardiac or pulmonary dysfunction or other significant systemic comorbidities.\n2. History of difficult airway management or congenital\u002Facquired structural anomalies of the airway.\n3. Active respiratory tract infection within 30 days preceding surgery.\n4. Preoperative neurological disorders or developmental abnormalities.\n5. Intraoperative occurrence of major complications necessitating deviation from the planned anesthesia protocol or surgical procedure.","6 Years",{"count":79,"type":21},350,[24],"The postoperative recovery period following general anesthesia has been associated with a 30%-50% incidence of postoperative respiratory adverse events (PRAEs) in pediatric populations, including laryngospasm, airway obstruction, and hypoxemia. Despite the limited effects of existing pharmacological and operative interventions, positional optimization (e.g., lateral or semirecumbent position) may play a potential role by decreasing airway resistance and improving oxygenation. However, evidence-based evidence for its use in pediatric populations is still lacking, necessitating the urgent need for randomized controlled trials.",[83,28,27,84],"Perioperative Respiratory Adverse Events","Children","2025-07-31",{"date":87,"type":37},"2025-08-06",{"date":89,"type":21},"2025-08-20",{"date":91,"type":21},"2026-08-27",{"name":93,"class":44},"Sichuan University"]