[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"pain-management-after-surgery\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:pain-management-after-surgery":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,45,73],{"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":28,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100620058","open-tap-block-in-pediatric-abdominal-surgery-100620058",false,"NCT07352683","Open TAP-block in Pediatric Abdominal Surgery","TAP-blockad Vid öppen Bukkirurgi Hos Barn","Inclusion Criteria:\n\n* Age 1-15 years\n* Scheduled for elective or acute open adominal surgical procedure\n\nExclusion Criteria:\n\n* chronic abdominal pain\n* known allergy to local analgetic\n* Stage 4 renal failure\n* psychiatric ailnment","ALL","1 Year","15 Years",{"count":20,"type":21},88,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this trial is to evaluate an open TAP-block vs continuous administration of local anestetic via a wound catheter for postoperative pain management in patients 1-15 years of age undergoing open abdominal surgery.",[27],"Pain Management After Surgery",[29,30,31],"pediatric","TAP-block","postoperative pain management","RECRUITING","2026-01-12",{"date":35,"type":36},"2026-01-20","ACTUAL",{"date":38,"type":36},"2025-12-01",{"date":40,"type":21},"2030-01-01",{"name":42,"class":43},"Uppsala University","OTHER",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":16,"minAge":52,"maxAge":53,"enrollmentInfo":54,"targetDuration":4,"studyType":22,"phases":56,"briefSummary":58,"conditions":59,"keywords":60,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":71,"locationsCount":44},"100570681","phase-4-the-effect-of-intraoperative-intravenous-lidocaine-infusion-on-postoperative-pain-and-recovery-in-children--7-years-old-undergoing-thoracoscopic-surgery-100570681","NCT06710405","The Effect of Intraoperative Intravenous Lidocaine Infusion on Postoperative Pain and Recovery in Children (\u003C 7 Years Old) Undergoing Thoracoscopic Surgery","The Effect of Intraoperative Intravenous Lidocaine Infusion on Postoperative Pain and Recovery in Children (\u003C 7 Years Old) Undergoing Thoracoscopic Surgery:Prospective, Randomized Controlled Trial","Inclusion Criteria:\n\n* Pediatric patients aged under 7 years undergoing thoracoscopic pulmonary resection\n\nExclusion Criteria:\n\n* cardiac dysfunction requiring vasopressors or inotropic agents\n* atrioventricular block or bradycardia\n* Liver or kidney dysfunction\n* Hypersensitivity to local anesthetics","6 Months","7 Years",{"count":55,"type":21},80,[57],"PHASE4","This study aims to investigate the efficacy of intraoperative intravenous lidocaine infusion on postoperative pain management and recovery in pediatric patients undergoing thoracoscopic pulmonary resection.",[27],[29,61,62,63],"thoracoscopic surgery","pain control","lidocaine","2025-05-11",{"date":66,"type":36},"2025-05-14",{"date":68,"type":36},"2024-12-09",{"date":70,"type":21},"2026-12-31",{"name":72,"class":43},"Seoul National University Hospital",{"id":74,"slug":75,"hasResults":11,"nctId":76,"briefTitle":77,"officialTitle":78,"acronym":4,"eligibilityCriteria":79,"healthyVolunteers":11,"sex":80,"minAge":4,"maxAge":81,"enrollmentInfo":82,"targetDuration":4,"studyType":22,"phases":84,"briefSummary":85,"conditions":86,"keywords":88,"overallStatus":90,"whyStopped":4,"lastUpdateSubmitDate":91,"lastUpdatePostDateStruct":92,"startDateStruct":94,"completionDateStruct":96,"leadSponsor":98,"locationsCount":44},"100575375","post-c-section-pain-control-satisfaction-with-erector-spinae-simple-block-vs-lateral-quadratus-lumborum-block-100575375","NCT06771466","Post-c-section Pain Control Satisfaction with Erector Spinae Simple Block Vs Lateral Quadratus Lumborum Block","Patients' Satisfaction for Pain Control Modalities After Caesarean Section Using Erector Spinae Plain Block Vs Lateral Quadratus Lumborum Block. a Randomized Clinical Trial","Inclusion Criteria:\n\n* Parturient female\n* Scheduled for elective cesarean section\n\nExclusion Criteria:\n\n* Known allergy to any of the medications used\n* Patients refused to participate in the study\n* Patients with emergency section,\n* Patients with Bleeding disease\n* Patients with postpartum haemorrhage","FEMALE","40 Years",{"count":83,"type":21},126,[24],"The study will compare the difference between the patient's satisfaction after Erector spinae plane block (ESP) and Quadratus Lumborum block lateral approach after caesarean section alone or as part of multimodal analgesia.\n\nThe primary outcome is to test whether the type of plane block has an implication on the patients' satisfaction.\n\nThe secondary outcome is to test the difference between the two approaches on the hospital discharge",[87,27],"Satisfaction",[89],"nerve block, pain, opioids, patient satisfaction, cesarean section","NOT_YET_RECRUITING","2025-01-10",{"date":93,"type":36},"2025-01-13",{"date":95,"type":21},"2025-03",{"date":97,"type":21},"2025-10",{"name":99,"class":43},"Wael Sayed El Gharabawy"]