[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"chronic-tonsillitis\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:chronic-tonsillitis":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,45],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":30,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":4},"100637115","recovery-from-tonsil-surgery-100637115",false,"NCT07598201","Recovery From Tonsil Surgery.","Recovery From Tonsil Surgery (FINITE-2). A Randomized, Controlled, Single-blinded Trial Exploring the Recovery and Effectiveness of Two Tonsil Surgery Techniques in Adults.","FINITE-2","Inclusion Criteria:\n\n1. Age 18-65 years\n2. Recurrent or chronic tonsillitis (see above)\n3. Indication for surgical treatment\n4. Eligible for day care surgery\n\nExclusion Criteria:\n\n1. Peritonsillar abscess less than month ago\n2. Previous palatine tonsil surgery (excluding small incision or biopsy)\n3. Current or positive history of a malignant disease\n4. Anticoagulant medication\n5. Contraindication to non-steroidal anti-inflammatory drugs (NSAID) or paracetamol\n6. Other significant co-morbidity\n7. Other contraindications determined by the investigator","ALL","18 Years","65 Years",{"count":21,"type":22},90,"ESTIMATED","INTERVENTIONAL",[25],"NA","The goal of this study is to optimize the duration of sick leave and the usage of opioids following partial tonsillar surgery in adults by comparing the recovery after extracapsular tonsillectomy (ECTE) with recovery after intracapsular tonsillectomy (ICTE). An additional objective is to confirm that ICTE is as effective as ECTE when comparing TOI-14 scores after 12 months post-operatively.\n\nThe main questions the study aims to answer are:\n\n* Is 10 days sick leave enough after partial tonsillectomy (ICTE)?\n* Are opioids needed at all after partial tonsillectomy (ICTE)?\n* Is ICTE as effective as ECTE when comparing TOI-14 symptom scores after 12 months from the surgery?\n\nAdult patients who are scheduled to tonsil surgery are randomised into 2 groups: ICTE and ECTE. Patients are blinded. Postoperatively they will answer structured questions about the recovery and effectiveness of the surgery. The last follow up survey is 60 months after the surgery.",[28,29],"Recurrent Tonsillitis","Chronic Tonsillitis",[31,32],"intracapsular tonsillectomy","extracapsular tonsillectomy","NOT_YET_RECRUITING","2026-05-19",{"date":36,"type":37},"2026-05-20","ACTUAL",{"date":39,"type":22},"2026-06-01",{"date":41,"type":22},"2030-12",{"name":43,"class":44},"Turku University Hospital","OTHER_GOV",{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":52,"minAge":18,"maxAge":4,"enrollmentInfo":53,"targetDuration":4,"studyType":55,"phases":4,"briefSummary":56,"conditions":57,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":63,"completionDateStruct":65,"leadSponsor":67,"locationsCount":4},"100546147","effect-of-osa-resulting-from-chronic-tonsillitis-on-pregnancy-outcomes-100546147","NCT06391151","Effect of OSA Resulting From Chronic Tonsillitis on Pregnancy Outcomes","Effect of Obstructive Sleep Apnea (OSA) Resulting From Chronic Tonsillitis on Pregnancy Outcomes","Inclusion Criteria:\n\n* Pregnant women confirmed with chronic tonsillitis by clinical diagnosis and presenting symptoms.\n* Pregnant women with a confirmed diagnosis of OSA based on polysomnography or other validated sleep monitoring techniques.\n* Pregnant women who are willing to participate in the study and provide informed consent.\n\nExclusion Criteria:\n\n* Pregnant women with other respiratory or sleep disorders that may confound the diagnosis of OSA.\n* Pregnant women with severe comorbidities or medical conditions that may significantly impact pregnancy outcomes.\n* Pregnant women who have undergone surgical treatment for chronic tonsillitis or OSA during the study period.\n* Pregnant women who refuse to participate in the study or are unable to provide informed consent.","FEMALE",{"count":54,"type":22},500,"OBSERVATIONAL","This cohort study aims to investigate the impact of obstructive sleep apnea hypopnea syndrome (OSA) resulting from chronic tonsillitis on pregnancy outcomes. The hypothesis posits that chronic tonsillitis-induced OSA may exacerbate pregnancy complications and increase the risk of adverse pregnancy outcomes.",[58,29,59],"Obstructive Sleep Apnea","Pregnancy","2024-06-03",{"date":62,"type":37},"2024-06-04",{"date":64,"type":22},"2024-07-01",{"date":66,"type":22},"2026-06-30",{"name":68,"class":69},"Peking University First Hospital","OTHER"]