[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"sacral-erector-spinae-plane-block\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:sacral-erector-spinae-plane-block":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,49,83,106],{"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":57,"maxAge":58,"enrollmentInfo":59,"targetDuration":4,"studyType":61,"phases":62,"briefSummary":64,"conditions":65,"keywords":66,"overallStatus":72,"whyStopped":4,"lastUpdateSubmitDate":73,"lastUpdatePostDateStruct":74,"startDateStruct":76,"completionDateStruct":78,"leadSponsor":80,"locationsCount":4},"100649185","ultrasound-guided-sacral-erector-spinae-plane-block-in-vnotes-surgery-100649185","NCT07732322","Ultrasound Guided Sacral Erector Spinae Plane Block in vNOTES Surgery","Ltrasound Guided Sacral Erector Spinae Plane Block in vNOTES Surgery","Inclusion Criteria:\n\n* Ages 18-65\n* Planned for elective vNOTES surgery\n* ASA 1-3\n* BMI \\\u003C35\n\nExclusion Criteria:\n\n* ASA 4\n* Planned emergency surgery\n* Pregnant patients\n* Persons with coagulopathy\n* Persons with allergy to local anesthetics\n* Persons with neurological disease\n* Persons with infection in the area where the block will be performed\n* Persons who refuse to participate in the study for any reason","FEMALE","18 Years","65 Years",{"count":60,"type":22},42,"INTERVENTIONAL",[63],"NA","Vaginal natural opening transendoscopic surgery (vNOTES) has emerged as a minimally invasive surgical approach in gynecological procedures. By utilizing the vaginal passage as a natural opening, vNOTES eliminates abdominal incisions and has been associated with less postoperative pain, shorter hospital stays, and faster recovery compared to traditional laparoscopic surgery. Despite these advantages, patients undergoing vNOTES may still experience significant perioperative pain due to visceral pelvic manipulation, colpotomy, and uterine traction during the procedure. Recently, sacral modification of ESP block has been described as a promising technique for surgeries involving sacral and perineal regions. Ultrasound-guided sacral ESP block has demonstrated beneficial postoperative analgesic effects in procedures such as pilonidal sinus surgery and other perineal operations. However, the potential role of sacral ESP block in gynecological procedures, particularly in vNOTES surgery, has not yet been sufficiently explored. Pelvic organs receive complex autonomic and somatic innervation, primarily originating from the sacral segments (S2-S4), including the pelvic splanchnic nerves and the pudendal nerve. Targeting these nerve pathways with sacral ESP block can provide effective analgesia for both the visceral and somatic components of pain associated with vNOTES procedures. Therefore, this prospective randomized study aimed to evaluate the effect of ultrasound-guided sacral erector spinae plane block on intraoperative opioid consumption in patients undergoing vNOTES surgery. It was hypothesized that adding sacral ESP block to general anesthesia would reduce intraoperative remifentanil requirements, lower postoperative pain scores, and decrease the amount of analgesics consumed postoperatively. The primary objective of this study was to investigate the effects of sacral ESP block on intraoperative opioid consumption in challenging vNOTES; the secondary objective was to determine its effects on postoperative pain scores and the amount of analgesics consumed.",[28],[67,68,69,70,71],"vNOTES","Sacral erector spinae plane block","Peripheral nerve block","Gynecological oncological surgery","Anesthesia","NOT_YET_RECRUITING","2026-07-28",{"date":75,"type":40},"2026-07-29",{"date":77,"type":22},"2026-07-25",{"date":79,"type":22},"2026-08-25",{"name":81,"class":82},"Seyyid Furkan Kına","OTHER_GOV",{"id":84,"slug":85,"hasResults":11,"nctId":86,"briefTitle":87,"officialTitle":88,"acronym":4,"eligibilityCriteria":89,"healthyVolunteers":11,"sex":90,"minAge":57,"maxAge":58,"enrollmentInfo":91,"targetDuration":4,"studyType":61,"phases":93,"briefSummary":94,"conditions":95,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":48},"100634038","sacral-erector-spinae-plane-block-in-pilonidal-sinus-surgery-100634038","NCT07534488","Sacral Erector Spinae Plane Block in Pilonidal Sinus Surgery","Evaluation of the Efficacy of Ultrasound-Guided Sacral Erector Spinae Plane Block in Postoperative Analgesia Management in Patients Undergoing Pilonidal Sinus Surgery","Inclusion Criteria:\n\n* Patients scheduled for elective pilonidal sinus surgery.\n* ASA physical status I and II\n\nExclusion Criteria:\n\n* Allergy or sensitivity to local anesthetics or opioid drugs.\n* Infection at the block site.\n* Alcohol or drug addiction.\n* Use of anticoagulant agents.\n* Patient refusal.","ALL",{"count":92,"type":22},60,[63],"This study aims to evaluate the efficacy of ultrasound-guided Sacral Erector Spinae Plane (ESP) block for postoperative analgesia management in patients undergoing pilonidal sinus surgery under general anesthesia",[28,96],"Pilonidal Sinus","2026-07-24",{"date":99,"type":40},"2026-07-27",{"date":101,"type":40},"2026-04-20",{"date":103,"type":22},"2026-09-15",{"name":105,"class":47},"Medipol University",{"id":107,"slug":108,"hasResults":11,"nctId":109,"briefTitle":110,"officialTitle":111,"acronym":4,"eligibilityCriteria":112,"healthyVolunteers":11,"sex":90,"minAge":18,"maxAge":113,"enrollmentInfo":114,"targetDuration":4,"studyType":61,"phases":115,"briefSummary":116,"conditions":117,"keywords":120,"overallStatus":72,"whyStopped":4,"lastUpdateSubmitDate":123,"lastUpdatePostDateStruct":124,"startDateStruct":126,"completionDateStruct":128,"leadSponsor":130,"locationsCount":48},"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","12 Years",{"count":92,"type":22},[63],"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.",[28,118,119],"Pediatric Regional Anesthesia","Regional Anaesthesia",[121,122],"pediatric regional anesthesia","sacral ESP","2025-12-23",{"date":125,"type":40},"2026-01-07",{"date":127,"type":22},"2026-01-01",{"date":129,"type":22},"2026-04-10",{"name":131,"class":47},"Istanbul University - Cerrahpasa"]