[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"orchiopexy\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:orchiopexy":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,49],{"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":23,"studyType":24,"phases":4,"briefSummary":25,"conditions":26,"keywords":31,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100651678","comparison-of-erector-spinae-plane-block-and-caudal-block-for-postoperative-analgesia-in-pediatric-patients-undergoing-orchiopexy-a-prospective-observational-study-100651678",false,"NCT07762339","Comparison of Erector Spinae Plane Block and Caudal Block for Postoperative Analgesia in Pediatric Patients Undergoing Orchiopexy: A Prospective Observational Study","Comparison of Erector Spinae Plane Block and Caudal Block for Postoperative Analgesia in Pediatric Patients Undergoing Orchiopexy","Inclusion Criteria:\n\n* Children aged 1 to 7 years with ASA physical status I-II undergoing unilateral orchiopexy surgery.\n\nExclusion Criteria:\n\n* ASA physical status ≥ III\n* History of prematurity (gestational age \\\u003C 37 weeks) Known coagulation disorders or bleeding tendency\n* Infection, inflammation, or skin lesion at the injection site\n* Known neurological or neuromuscular diseases\n* Presence of significant cardiac or pulmonary disease (e.g., congenital heart disease, active asthma)\n* Hepatic or renal dysfunction\n* Known allergy or hypersensitivity to local anesthetics (e.g., bupivacaine, lidocaine)\n* Developmental delay or cognitive impairment that prevents accurate pain assessment\n* Use of additional regional analgesia techniques (e.g., caudal block) during surgery\n* Block failure or intraoperative complications requiring exclusion from protocol analysis\n* Lack of parental consent for participation in the study",true,"MALE","1 Year","7 Years",{"count":21,"type":22},84,"ESTIMATED","1 Day","OBSERVATIONAL","This study aims to compare the analgesic efficacy of ultrasound-guided erector spinae plane block and caudal block for postoperative pain management in pediatric patients undergoing orchiopexy. Postoperative pain scores, time to first rescue analgesic requirement, total analgesic consumption, and block-related adverse effects will be evaluated during the first 24 hours after surgery. The study will assess whether erector spinae plane block provides effective postoperative analgesia comparable to or superior to caudal block in pediatric orchiopexy.",[27,28,29,30],"Caudal Epidural Anesthesia","Sacral Erector Spinae Plane Block","Orchiopexy","FLACC Scale",[32,33,34,35],"FLACC SCALE","caudal epidural anesthesia","sacral erector spinae plane block","orchiopexy","RECRUITING","2026-08-12",{"date":39,"type":40},"2026-08-13","ACTUAL",{"date":42,"type":40},"2026-06-08",{"date":44,"type":22},"2027-01-08",{"name":46,"class":47},"Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization","OTHER",1,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":4,"eligibilityCriteria":55,"healthyVolunteers":11,"sex":56,"minAge":18,"maxAge":19,"enrollmentInfo":57,"targetDuration":23,"studyType":24,"phases":4,"briefSummary":59,"conditions":60,"keywords":4,"overallStatus":61,"whyStopped":4,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":4},"100593469","comparison-of-analgesic-efficacy-of-fascia-transversalis-plan-block-and-caudal-epidural-block-in-pediatric-patients-undergoing-orchiopexy-100593469","NCT07006844","Comparison of Analgesic Efficacy of Fascia Transversalis Plan Block and Caudal Epidural Block in Pediatric Patients Undergoing Orchiopexy","Comparison of Analgesic Efficacy of Fascia Transversalis Plan Block and Caudal Epidural Block in Pediatric Patients Undergoing Orchiopexy. Our Study, it Was Planned to Compare the Postoperative Analgesic Efficacy of Routinely Applied Fascia Transversalis Plan Block and Caudal Epidural Block for Analgesia After General Anesthesia in Pediatric Patients Undergoing Orchiopexy (Unilateral) According to the Surgery and Suitability of the Patient and the Competence of the Anesthesiologist","Inclusion Criteria:\n\nASA I-II, patients who will undergo unilateral orchiopexy under general anesthesia patients between the ages of 1-7 years, who have no contraindications for block application, and whose participation in the study is accepted by their legal guardian will be included in the study.\n\nExclusion Criteria:\n\nLack of consent by the patient's legal guardian, contraindications for block (bleeding diathesis, regional infection, neuromuscular disease), patients over 7 years of age","ALL",{"count":58,"type":22},60,"Orchiopexy is a surgery with a high frequency in the pediatric population. The use of regional anesthesia techniques has become widespread and its importance has increased in order to provide more effective and prolonged perioperative analgesia, as well as to prevent the side effects of opioids such as respiratory depression and to reduce systemic analgesic consumption. In this study, it was planned to compare the postoperative analgesic efficacy of routinely applied fascia transversalis plan block and caudal epidural block for analgesia after general anesthesia in pediatric patients undergoing orchiopexy (unilateral) according to the surgery and suitability of the patient and the competence of the anesthesiologist.\n\nASA I-II, patients who will undergo unilateral orchiopexy under general anesthesia, patients between the ages of 1-7 years, who have no contraindications for block application, and whose participation in the study is accepted by their legal guardian will be included in the study. After induction of general anesthesia and ensuring airway safety with a laryngeal mask, one of the regional anesthesia methods (fascia transversalis plan block or caudal epidural block) deemed appropriate for the patient is applied by the specialist of the room before the surgical incision. Postoperative analgesic needs of the patients and FLACC score will be evaluated at 30 minutes, 1, 2, 4, 6, 12 and 24 hours postoperatively.",[29],"NOT_YET_RECRUITING","2025-06-04",{"date":64,"type":40},"2025-06-05",{"date":66,"type":22},"2025-06-07",{"date":68,"type":22},"2026-01-07",{"name":46,"class":47}]