[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"emergence-delirium-in-pediatric-anesthesia\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:emergence-delirium-in-pediatric-anesthesia":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,52,78,110,140],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":32,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":40,"lastUpdatePostDateStruct":41,"startDateStruct":44,"completionDateStruct":46,"leadSponsor":48,"locationsCount":51},"100634074","the-effect-of-paedfusor-tci-eleveld-tci-and-sevoflurane-anesthesia-on-postoperative-awakening-agitation-in-pediatric-patients-100634074",false,"NCT07534956","The Effect of Paedfusor TCI, Eleveld TCI, and Sevoflurane Anesthesia on Postoperative Awakening Agitation in Pediatric Patients","Investigation of the Effects of Two Different TCI (Target Controlled Infusion) Models (Paedfusor and Eleveld) and Inhalation Anesthesia on Postoperative Awakening Agitation\u002FDelirium in Pediatric Patients","Inclusion Criteria:\n\n* Children aged 3-10 years\n* Children weighing over 10 kg\n* American Society of Anesthesiologists (ASA) physical condition classification I-II\n* Those who will undergo planned urogenital surgery under general anesthesia\n* Those who have obtained written informed consent from their parents or legal guardians\n\nExclusion Criteria:\n\n* Patients assessed as ASA III or higher\n* Known neurological or psychiatric disorders\n* Developmental delay or cognitive impairment\n* Use of sedatives or psychoactive drugs\n* Allergy or contraindication to the study drugs (propofol or sevoflurane)\n* History of previous adverse reactions to anesthesia\n* Patients requiring emergency surgery\n* Significant liver, kidney, or cardiovascular disease\n* Patients whose parents or legal guardians have not given consent",true,"ALL","3 Years","10 Years",{"count":21,"type":22},150,"ESTIMATED","INTERVENTIONAL",[25],"NA","Emergence delirium is a common complication in pediatric patients undergoing general anesthesia. The aim of this study is to investigate the incidence of postoperative awakening delirium and agitation in pediatric patients aged 3-10 years (ASA I-II) using two different target-controlled infusion (TCI) methods (Paedfusor and Eleveld) for TIVA, compared to inhalation anesthesia. This study will examine the effect of two different TCI models on postoperative awakening agitation\u002Fdelirium by comparing them with each other and with inhalation anesthesia.",[28,29,30,31],"Emergence Delirium in Pediatric Anesthesia","Pediatric Anesthesia","Postoperative Agitations in Pediatric Patients","Postoperative Nausea and Vomiting (PONV)",[33,34,35,36,37,38],"pediatric anesthesia","paedfusor","eleveld","target controlled infusion","sevoflurane","postoperative agitation","RECRUITING","2026-04-11",{"date":42,"type":43},"2026-04-16","ACTUAL",{"date":45,"type":43},"2026-01-13",{"date":47,"type":22},"2027-11-30",{"name":49,"class":50},"Marmara University Pendik Training and Research Hospital","OTHER",2,{"id":53,"slug":54,"hasResults":11,"nctId":55,"briefTitle":56,"officialTitle":56,"acronym":4,"eligibilityCriteria":57,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":58,"enrollmentInfo":59,"targetDuration":4,"studyType":23,"phases":61,"briefSummary":63,"conditions":64,"keywords":65,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":77},"100632913","phase-2-the-effect-of-dormicum-ketamine-versus-dexmedetomidine-on-emergence-delirium-during-deep-sedation-in-paediatric-burn-patients-100632913","NCT07519863","The Effect of Dormicum-Ketamine Versus Dexmedetomidine on Emergence Delirium During Deep Sedation in Paediatric Burn Patients","Inclusion Criteria:\n\n* Age from 3 to 16 years\n* Both sexes\n* Patients classified as American Society of Anesthesiologists (ASA) Physical -Status I-II\n* Patients scheduled for elective burn-related procedures (e.g., burn dressing changes or minor interventions)\n\nExclusion Criteria:\n\n* Refusal or inability to provide written informed consent from parent or legal guardian\n* Known allergy or hypersensitivity to any of the study medications (midazolam, ketamine, or dexmedetomidine)\n* Presence of hepatic dysfunction\n* Presence of renal dysfunction\n* Presence of immunological or hematological disorders\n* History of epilepsy, developmental delay (mental retardation), or neurological deficits\n* Patients receiving or requiring high doses of inotropes and\u002For vasopressors intraoperatively or postoperatively\n* Preoperative hemodynamic instability, defined as uncontrolled hypertension, hypotension, or bradycardia","16 Years",{"count":60,"type":22},60,[62],"PHASE2","The aim of this study is to compare the effects of dormicum-ketamine versus dexmedetomidine on postoperative emergence delirium in pediatric patients undergoing deep sedation for burn-related procedures",[28],[66,67],"Dexmedetomidine","Burn Procedural sedation","2026-04-02",{"date":70,"type":43},"2026-04-09",{"date":72,"type":43},"2025-11-20",{"date":74,"type":22},"2026-12",{"name":76,"class":50},"Ain Shams University",1,{"id":79,"slug":80,"hasResults":11,"nctId":81,"briefTitle":82,"officialTitle":83,"acronym":4,"eligibilityCriteria":84,"healthyVolunteers":16,"sex":17,"minAge":85,"maxAge":86,"enrollmentInfo":87,"targetDuration":4,"studyType":23,"phases":89,"briefSummary":90,"conditions":91,"keywords":97,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":101,"lastUpdatePostDateStruct":102,"startDateStruct":104,"completionDateStruct":106,"leadSponsor":108,"locationsCount":77},"100626441","efficacy-of-ultrasound-guided-greater-auricular-nerve-block-in-preventing-postoperative-emergence-agitation-in-pediatric-patients-undergoing-microscopic-middle-ear-surgery-100626441","NCT07435675","Efficacy of Ultrasound-guided Greater Auricular Nerve Block in Preventing Postoperative Emergence Agitation in Pediatric Patients Undergoing Microscopic Middle Ear Surgery.","Efficacy of Ultrasound-guided Greater Auricular Nerve Block in Preventing Postoperative Emergence Agitation in Pediatric Patients Undergoing Microscopic Middle Ear Surgery: A PROSPECTIVE RANDOMIZED DOUBLE- BLINDED CLINICAL TRIAL","Inclusion Criteria:\n\n* Age between 5 and 14 years (preschool to early school age group at highest risk for EA).\n* ASA physical status I or II.\n* Scheduled for elective microscopic middle ear surgery under general anesthesia (e.g., tympanoplasty, myringoplasty).\n* Ability to comply with FLACC and PAED scoring during postoperative period.\n* Informed consent obtained from a parent or legal guardian.\n\nExclusion Criteria:\n\n* Known neurological, developmental, or psychiatric disorders (e.g., autism, ADHD, seizure disorder).\n* Known hypersensitivity to amide local anesthetics (e.g., lidocaine, bupivacaine).\n* Skin infection, hematoma, or trauma at or near the proposed block site.\n* Non-elective (emergency) or combined surgeries.\n* Inability to assess pain or agitation due to hearing loss, or communication impairment.\n* Parental or legal guardian refusal to participate.","5 Years","14 Years",{"count":88,"type":22},74,[25],"This study is designed to evaluate the effectiveness of ultrasound-guided greater auricular nerve block (GAN) on the reduction of emergence agitation (EA) occurrence and EA severity in children who are receiving general anesthesia for a microscopic middle ear operation.",[92,93,94,95,28,96],"Emergence Agitation","Emergence Delirium, Anesthesia","Emergence From Anesthesia","Emergence Delirium","Emergence Agitation, Post Operative Behavioral Changes",[98,99,100],"emergence agitation","emergence delirium","EA","2026-02-23",{"date":103,"type":43},"2026-02-27",{"date":105,"type":43},"2025-08-01",{"date":107,"type":22},"2026-04-01",{"name":109,"class":50},"Fayoum University",{"id":111,"slug":112,"hasResults":11,"nctId":113,"briefTitle":114,"officialTitle":115,"acronym":4,"eligibilityCriteria":116,"healthyVolunteers":16,"sex":117,"minAge":18,"maxAge":118,"enrollmentInfo":119,"targetDuration":121,"studyType":122,"phases":4,"briefSummary":123,"conditions":124,"keywords":126,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":131,"lastUpdatePostDateStruct":132,"startDateStruct":134,"completionDateStruct":136,"leadSponsor":138,"locationsCount":77},"100623985","ride-on-toy-car-use-during-operating-room-transfer-in-preschool-children-100623985","NCT07403747","Ride-On Toy Car Use During Operating Room Transfer in Preschool Children","Evaluation of the Effects of Ride-On Toy Car Use During Operating Room Transfer on Preoperative Anxiety and Postoperative Delirium in Preschool Children","Inclusion Criteria:\n\n* Male children aged 3 to 7 years scheduled for elective adenoidectomy and\u002For tonsillectomy under general anesthesia\n* Ability to communicate verbally\n* American Society of Anesthesiologists (ASA) physical status I or II\n* Written informed consent obtained from a parent or legal guardian\n\nExclusion Criteria:\n\n* Presence of psychiatric disorders, genetic diseases, neurological or developmental disorders\n* Chronic pain conditions or ongoing medical treatments that may affect anxiety levels\n* Refusal to participate despite repeated encouragement by the investigators\n* Use of additional anxiolytic interventions or medications prior to the intervention outside the study protocol\n* Previous history of surgical procedures","MALE","7 Years",{"count":120,"type":22},96,"1 Day","OBSERVATIONAL","The goal of this clinical trial is to determine whether the method of transfer to the operating room can reduce preoperative anxiety and postoperative emergence delirium in male children aged 3 to 7 years undergoing elective adenoidectomy and\u002For tonsillectomy.\n\nThe main questions it aims to answer are:\n\n* Does transfer using a ride-on toy car reduce preoperative anxiety compared with standard stretcher transfer?\n* Does this transfer method affect the incidence and severity of postoperative emergence delirium? Researchers will compare toy car transfer with standard hospital stretcher transfer to see if the toy car transfer is associated with lower anxiety levels and reduced emergence delirium.\n\nParticipants will:\n\n* Transfer to the operating room either using a ride-on toy car or a standard hospital stretcher\n* Have preoperative anxiety assessed at predefined time points\n* Be evaluated for postoperative emergence delirium during recovery",[125,28],"Preoperative Anxiety",[127,128,129,130],"Pediatric anesthesia","Preoperative anxiety","Toy car intervention","Emergence delirium","2026-02-05",{"date":133,"type":43},"2026-02-11",{"date":135,"type":43},"2025-11-01",{"date":137,"type":22},"2026-04-30",{"name":139,"class":50},"Ankara City Hospital Bilkent",{"id":141,"slug":142,"hasResults":11,"nctId":143,"briefTitle":144,"officialTitle":145,"acronym":4,"eligibilityCriteria":146,"healthyVolunteers":16,"sex":147,"minAge":18,"maxAge":118,"enrollmentInfo":148,"targetDuration":121,"studyType":122,"phases":4,"briefSummary":150,"conditions":151,"keywords":152,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":131,"lastUpdatePostDateStruct":153,"startDateStruct":154,"completionDateStruct":156,"leadSponsor":158,"locationsCount":77},"100623987","personal-versus-hospital-provided-dolls-in-preschool-children-100623987","NCT07403773","Personal Versus Hospital-Provided Dolls in Preschool Children","Comparison of the Effects of Personal Versus Hospital-Provided Dolls on Preoperative Anxiety and Postoperative Delirium in Preschool Children","Inclusion Criteria:\n\n* Female children aged 3-7 years\n* Scheduled for elective adenoidectomy and\u002For tonsillectomy under general anesthesia\n* Able to communicate verbally\n* ASA physical status I or II, according to the American Society of Anesthesiologists classification\n* Written informed consent obtained from a parent or legal guardian\n\nExclusion Criteria:\n\n* Presence of psychiatric, neurological, or developmental disorders\n* Presence of chronic pain or ongoing medical treatment that may affect anxiety levels\n* Refusal to participate despite repeated encouragement by the investigators\n* Use of additional anxiety-reducing methods or medications outside the study protocol prior to intervention\n* Previous surgical experience","FEMALE",{"count":149,"type":22},120,"The goal of this study is to evaluate the effects of personal versus hospital-provided dolls on preoperative anxiety and postoperative delirium in preschool children aged 3-7 years undergoing elective adenoidectomy and\u002For tonsillectomy.\n\nThe main questions it aims to answer are:\n\n* Is the use of a personal doll or a hospital-provided doll associated with lower preoperative anxiety compared with no doll use?\n* Is dolls used associated with a reduced incidence and severity of postoperative emergence delirium?\n* Researchers will compare children accompanied by a hospital-provided doll, children accompanied by their personal doll, and children with no doll to assess differences in preoperative anxiety levels, serum cortisol concentrations, and postoperative delirium scores.\n\nParticipants will:\n\n* Be observed in one of three exposure groups (hospital-provided doll, personal doll, or no doll)\n* Undergo standardized preoperative anxiety assessments at predefined time points\n* Have serum cortisol levels measured during routine intravenous cannulation\n* Be assessed for postoperative delirium in the recovery unit",[125,28],[125,95,29],{"date":133,"type":43},{"date":155,"type":43},"2026-02-01",{"date":157,"type":22},"2026-07-30",{"name":139,"class":50}]