[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"pediatric-regional-anesthesia\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:pediatric-regional-anesthesia":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,48],{"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":30,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100647730","retrolaminar-plane-block-versus-anterior-quadratus-lumborum-block-in-pediatric-urogenital-surgery-100647730",false,"NCT07711496","Retrolaminar Plane Block Versus Anterior Quadratus Lumborum Block in Pediatric Urogenital Surgery","Comparison of the Postoperative Analgesic Efficacy of Retrolaminar Plane Block and Anterior Quadratus Lumborum Block in Pediatric Lower Urogenital Surgery: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Age between 6 months and 12 years\n* Scheduled for lower abdominal urogenital surgery (e.g., inguinal hernia repair or orchiopexy for undescended testis)\n* American Society of Anesthesiologists physical status classification I-III\n* Written informed consent obtained from a parent or legal guardian\n\nExclusion Criteria:\n\n* History of allergy to local anesthetic agents\n* Presence of infection at the planned injection site\n* Coagulopathy or any other condition contraindicating regional anesthesia\n* Planned laparoscopic orchiopexy\n* American Society of Anesthesiologists physical status classification IV\n* Inability to obtain informed consent from a parent or legal guardian\n* Anticipated requirement for postoperative intensive care unit admission","ALL","6 Months","12 Years",{"count":20,"type":21},76,"ESTIMATED","INTERVENTIONAL",[24],"NA","Effective control of postoperative pain following pediatric lower urogenital surgery is important for enhancing recovery and reducing opioid requirements. Anterior quadratus lumborum block and retrolaminar block are two ultrasound-guided truncal block techniques used for perioperative analgesia in lower abdominal surgery. However, direct comparisons of their analgesic efficacy in pediatric lower urogenital procedures remain limited.\n\nThis prospective, randomized, controlled trial will enroll 76 pediatric patients aged 6 months to 12 years with American Society of Anesthesiologists physical status I-III who are scheduled for elective lower urogenital surgery. Participants will be randomly assigned in a 1:1 ratio to receive either an anterior quadratus lumborum block or a retrolaminar block. Both techniques will be performed under ultrasound guidance in addition to standardized general anesthesia.\n\nThe primary outcome will be rescue analgesic requirement during the first 24 postoperative hours. Secondary outcomes will include postoperative pain scores, time to first rescue analgesic administration, intraoperative remifentanil consumption, adverse effects such as nausea and vomiting, and caregiver satisfaction. The study aims to compare the postoperative analgesic efficacy and safety of anterior quadratus lumborum block and retrolaminar block in pediatric patients undergoing lower urogenital surgery.",[27,28,29],"Pediatric Regional Anesthesia","Retrolaminar Block","Pediatric Postoperative Pain",[31,32,33,34],"pediatric anesthesia","pediatric regional anesthesia","retrolaminar block","pediatric pain management","NOT_YET_RECRUITING","2026-07-14",{"date":38,"type":39},"2026-07-17","ACTUAL",{"date":41,"type":21},"2026-07-25",{"date":43,"type":21},"2027-09-01",{"name":45,"class":46},"Istanbul University - Cerrahpasa","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":16,"minAge":55,"maxAge":18,"enrollmentInfo":56,"targetDuration":4,"studyType":22,"phases":58,"briefSummary":59,"conditions":60,"keywords":63,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":47},"100617676","sacral-erector-spinae-plane-block-versus-penile-block-for-analgesia-in-pediatric-circumcision-100617676","NCT07321717","Sacral Erector Spinae Plane Block Versus Penile Block For Analgesia In Pediatric Circumcision","A Randomized Controlled Trial Comparing The Analgesic Effectiveness Of Sacral Erector Spinae Plane Block And Penile Block In Children Undergoing Circumcision Surgery","Inclusion Criteria:\n\n* Age between 1 and 12 years\n* Scheduled for circumcision surgery\n* Classified as American Society of Anesthesiologists (ASA) physical status I-II\n* Written informed consent obtained from both the participant (when appropriate) and their parents or legal guardians\n\nExclusion Criteria:\n\n* Age under 1 year or over 12 years\n* Undergoing circumcision combined with other surgical procedures\n* Presence of neurological deficits\n* History of bleeding diathesis\n* Allergy to local anesthetic (LA) drugs\n* Redness or infection at the injection site\n* Presence of congenital sacral anomalies\n* Mental retardation\n* Psychiatric disorders or kidney disease\n* Refusal to participate in the study","1 Year",{"count":57,"type":21},60,[24],"Circumcision is one of the most frequently performed surgical procedures in childhood and is associated with significant postoperative pain. This randomized controlled trial (RCT) aims to compare the analgesic effectiveness of sacral erector spinae plane block (sacral ESPB) and penile nerve block (PNB) in children undergoing circumcision surgery. The primary outcome is postoperative pain, assessed using the Face, Legs, Activity, Cry, and Consolability (FLACC) scale at predefined time intervals within the first 24 hours after surgery. Secondary outcomes include intraoperative analgesic consumption, time to first postoperative analgesic requirement, perioperative hemodynamic changes. The results of this study are expected to provide evidence for selecting the optimal regional analgesic technique for pediatric circumcision surgery.",[61,27,62],"Sacral Erector Spinae Plane Block","Regional Anaesthesia",[32,64],"sacral ESP","2025-12-23",{"date":67,"type":39},"2026-01-07",{"date":69,"type":21},"2026-01-01",{"date":71,"type":21},"2026-04-10",{"name":45,"class":46}]