[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100644743":3},{"organization":4,"armGroups":7,"interventions":10,"overallOfficials":10,"centralContacts":15,"locations":21,"responsibleParty":35,"collaborators":10,"id":39,"slug":10,"hasResults":40,"nctId":41,"briefTitle":42,"officialTitle":43,"acronym":10,"eligibilityCriteria":44,"healthyVolunteers":40,"sex":45,"minAge":46,"maxAge":47,"enrollmentInfo":48,"targetDuration":10,"studyType":51,"phases":10,"briefSummary":52,"conditions":53,"keywords":10,"overallStatus":57,"whyStopped":10,"lastUpdateSubmitDate":58,"lastUpdatePostDateStruct":59,"startDateStruct":62,"completionDateStruct":64,"leadSponsor":66,"locationsCount":67},{"fullName":5,"class":6},"Baylor College of Medicine","OTHER",[8,12],{"label":9,"type":10,"description":11,"interventionNames":10},"Cohort 1: Acetaminophen + Ibuprofen",null,"Participants prescribed acetaminophen and ibuprofen after discharge according to routine clinical practice.",{"label":13,"type":10,"description":14,"interventionNames":10},"Cohort 2: Acetaminophen + Oral Ketorolac","Participants prescribed acetaminophen and low-dose oral ketorolac after discharge according to routine clinical practice.",[16],{"name":17,"role":18,"phone":19,"phoneExt":10,"email":20},"Adam C Adler, MD","CONTACT","8328245800","adam.adler@bcm.edu",[22],{"facility":23,"status":10,"city":24,"state":25,"zip":26,"country":27,"countryCode":28,"cosmosGeoPoint":29,"geoPoint":34,"contacts":10},"Baylor College of Medicine\u002F Texas Childrens Hospital","Houston","Texas","77030","United States","US",{"type":30,"coordinates":31},"Point",[32,33],-95.36327,29.76328,{"lat":33,"lon":32},{"type":36,"investigatorFullName":37,"investigatorTitle":38,"investigatorAffiliation":5,"oldNameTitle":10,"oldOrganization":10},"PRINCIPAL_INVESTIGATOR","Adam Adler MD, MS, FAAP","Professor of Anesthesiology and Surgery","100644743",false,"NCT07672418","Postoperative Pain After Pediatric Adenotonsillectomy With Ketorolac or Ibuprofen","Assessment of Postoperative Pain Outcomes Following Pediatric Adenotonsillectomy and the Impact on Non-Steroidal Anti-Inflammatory Drugs","Inclusion Criteria:\n\nScheduled for outpatient adenotonsillectomy Age 13-18 years ASA physical status I-III Patient or parent has access to a phone with text-messaging capability Patient assent Parent or legal guardian consent\n\nExclusion Criteria:\n\nInpatient admission or planned 23-hour observation Known hematologic condition or prior bleeding disorder Current anticoagulant use Known or suspected chronic kidney disease or solitary kidney Known or suspected liver disease or prior liver transplant Known or suspected mitochondrial disease or genetic anomaly Inability to self-report pain History of gastrointestinal ulcer or bleeding Allergy to acetaminophen, ibuprofen, or ketorolac Non-English or non-Spanish speaking Chronic pain or condition requiring frequent routine NSAID use Patient refusal Parent or guardian refusal","ALL","13 Years","18 Years",{"count":49,"type":50},200,"ESTIMATED","OBSERVATIONAL","This prospective observational study will evaluate postoperative pain after outpatient pediatric adenotonsillectomy in adolescents prescribed either acetaminophen with ibuprofen or acetaminophen with oral ketorolac after discharge, based on the prescribing preference of the otolaryngology surgeon. Participants will complete text-message surveys after discharge to assess pain severity, medication administration, and functional recovery for up to 14 days.",[54,55,56],"Sleep","Pediatrics","Adenotonsillectomy","NOT_YET_RECRUITING","2026-06-23",{"date":60,"type":61},"2026-06-29","ACTUAL",{"date":63,"type":50},"2026-06-24",{"date":65,"type":50},"2027-06-30",{"name":5,"class":6},1]