[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100602199":3},{"organization":4,"armGroups":7,"interventions":10,"overallOfficials":10,"centralContacts":12,"locations":22,"responsibleParty":37,"collaborators":10,"id":41,"slug":42,"hasResults":43,"nctId":44,"briefTitle":45,"officialTitle":46,"acronym":10,"eligibilityCriteria":47,"healthyVolunteers":43,"sex":48,"minAge":49,"maxAge":50,"enrollmentInfo":51,"targetDuration":10,"studyType":54,"phases":10,"briefSummary":55,"conditions":56,"keywords":58,"overallStatus":61,"whyStopped":10,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":71},{"fullName":5,"class":6},"Kocaeli University","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":10},"Postoperative pediatric patients aged 8-17",null,"Children aged 8 to 17 years who have undergone surgery and voluntarily agree to participate in the study for a period of six months will be included.\n\nTo evaluate pain intensity, the Numeric Rating Scale (NRS) will be utilized, while the Pediatric Quality of Life Inventory 4.0 (PedsQL) will be used to assess quality of life.\n\nThe assessment parameters will be administered at multiple time points: in the preoperative period, at discharge, and on postoperative day 7, as well as at 1 month, 3 months, and 6 months following surgery.",[13,18],{"name":14,"role":15,"phone":16,"phoneExt":10,"email":17},"Onur ERDEM, Medical Doctor","CONTACT","+905526904115","mdonurerdem@gmail.com",{"name":19,"role":15,"phone":20,"phoneExt":10,"email":21},"Can AKSU, Associate Professor","+905332568290","dr.aksu@gmail.com",[23],{"facility":24,"status":10,"city":25,"state":26,"zip":27,"country":28,"countryCode":10,"cosmosGeoPoint":29,"geoPoint":34,"contacts":35},"Kocaeli University Faculty of Medicine","Kocaeli","Izmit","41100","Turkey (Türkiye)",{"type":30,"coordinates":31},"Point",[32,33],27.51145,39.62497,{"lat":33,"lon":32},[36],{"name":14,"role":15,"phone":16,"phoneExt":10,"email":17},{"type":38,"investigatorFullName":39,"investigatorTitle":40,"investigatorAffiliation":5,"oldNameTitle":10,"oldOrganization":10},"PRINCIPAL_INVESTIGATOR","Onur ERDEM","Research Assistant Doctor","100602199","postoperative-chronic-pain-in-children-aged-8-to-17-100602199",false,"NCT07120399","Postoperative Chronic Pain in Children Aged 8 to 17","Investigation of the Incidence of Postoperative Chronic Pain in Children Aged 8 to 17 Years","Inclusion Criteria:\n\n* Voluntary participation\n* Undergoing a surgical procedure under anesthesia at our hospital\n* Availability of complete patient data for a 6-month postoperative follow-up period\n\nExclusion Criteria:\n\n* Presence of speech or communication disorders\n* Development of postoperative complications\n* Undergoing any additional surgical procedure for any reason during the 6 months follow-up period\n* Having diagnosed psychiatric or neurological disorders\n* Having a pre-existing history of chronic or long-term pain","ALL","8 Years","17 Years",{"count":52,"type":53},323,"ESTIMATED","OBSERVATIONAL","The objective of this study is to assess the incidence of chronic postoperative pain in pediatric patients aged 8 to 17 years following surgical procedures. Furthermore, it seeks to identify potential risk factors contributing to the development of such pain and to evaluate its long-term implications.",[57],"Postoperative Chronic Pain",[59,57,60],"Pain","Quality of Life","NOT_YET_RECRUITING","2025-08-12",{"date":64,"type":65},"2025-08-14","ACTUAL",{"date":67,"type":53},"2025-08-15",{"date":69,"type":53},"2026-08-15",{"name":5,"class":6},1]