[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"San Giovanni di Dio Hospital\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":92},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,42,66],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":26,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":41},"100640758","deep-rectus-sheath-drs-block-in-abdominal-surgery-100640758",false,"NCT07586462","Deep Rectus Sheath (DRS) Block in Abdominal Surgery","The Effectiveness of the Deep Rectus Sheath (Preperitoneal) Block for Postoperative Analgesia in Abdominal Surgery: A Prospective Observational Clinical Study","DRS block","Inclusion Criteria:\n\n* Age ≥ 18 years\n* Patients undergoing abdominal surgery, either open or laparoscopic\n* ASA physical status I-III\n* Neuraxial or general anesthesia according to standard clinical practice\n* Provision of informed consent to participate in the study\n\nExclusion Criteria:\n\n* Refusal to provide informed consent\n* Contraindications to locoregional anesthesia\n* Known allergy to local anesthetic agents\n* Coagulation disorders or incompatible anticoagulant therapy\n* Infection at the injection site\n* Cognitive impairment preventing reliable assessment of outcomes","ALL",{"count":19,"type":20},60,"ESTIMATED","OBSERVATIONAL","The goal of this observational study is to learn about the effectiveness of the Deep Rectus Sheath (Preperitoneal) block in patients undergoing abdominal surgery. The main question it aims to answer is:\n\nDoes the Deep Rectus Sheath block improve postoperative recovery and pain control compared to standard care or other fascial plane blocks in patients undergoing abdominal surgery?\n\nParticipants undergoing open or laparoscopic abdominal surgery as part of their routine clinical care will receive analgesic management according to standard practice, which may include systemic analgesia alone, Deep Rectus Sheath block, or other fascial plane blocks (such as TAP, ESP, or QL), depending on anesthesiologist choice. Postoperative outcomes will be collected prospectively, including quality of recovery (QoR-15 at 24 hours), pain scores at rest and during movement up to 48 hours, analgesic consumption, time to first analgesic request, mobilization time, and occurrence of complications.",[24,25],"Laparoscopy","Abdominal Surgery by Laparotomy",[27,28,24],"rectus sheath","fascial blocks","RECRUITING","2026-05-18",{"date":32,"type":33},"2026-05-22","ACTUAL",{"date":35,"type":20},"2026-05",{"date":37,"type":20},"2027-05",{"name":39,"class":40},"San Giovanni di Dio Hospital","OTHER",2,{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":47,"acronym":48,"eligibilityCriteria":49,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":50,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":52,"conditions":53,"keywords":56,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":61,"startDateStruct":62,"completionDateStruct":63,"leadSponsor":65,"locationsCount":41},"100637466","the-quadro-iliac-plane-qip-block-in-hip-arthroplasty-100637466","NCT07591311","The Quadro-Iliac Plane (QIP) Block in Hip Arthroplasty","The Effectiveness of the \"Quadro-Iliac Plane Block\" in Hip Arthroplasty: A Prospective Observational Clinical Study","QIP in hip","Inclusion Criteria:\n\n* Age ≥ 18 years\n* Patients undergoing hip arthroplasty surgery, either elective or for a proximal femoral fracture\n* Expected postoperative hospital stay ≥ 24 hours\n* ASA physical status I-III\n* Neuraxial and\u002For locoregional anesthesia according to standard clinical practice\n* Provision of informed consent to participate in the study\n\nExclusion Criteria:\n\n* Absence of informed consent\n* Contraindications to locoregional and\u002For spinal anesthesia\n* Allergy to local anesthetic agents\n* Cognitive impairment preventing reliable assessment of outcomes\n* Coagulation disorders and\u002For platelet abnormalities\n* Antiplatelet or anticoagulant therapy that contraindicates spinal anesthesia\n* Presence of localized infection or sepsis at the sites to be treated",{"count":51,"type":20},80,"The goal of this observational study is to learn about the effectiveness of different locoregional anesthesia techniques, particularly the Quadro-Iliac Plane (QIP) block, in patients undergoing total hip arthroplasty. The main question it aims to answer is:\n\nDoes the QIP block improve postoperative recovery and pain control compared to other routinely used locoregional anesthesia techniques in patients undergoing hip replacement surgery?\n\nParticipants undergoing hip arthroplasty as part of their standard clinical care will receive one of the locoregional anesthesia techniques already in use at the hospital (including QIP block, fascia iliaca block, PENG block, or others, according to anesthesiologist choice). Postoperative outcomes will be collected prospectively, including quality of recovery (QoR-15 at 24 hours), pain scores at rest and during movement at predefined time points up to 48 hours, analgesic consumption, time to first analgesic request, time to mobilization, and occurrence of complications.",[54,55],"Hip Surgery","Hip Arthroplasty",[57,58,59,60],"regional anesthesia","hip","hip fracture","QIP",{"date":32,"type":33},{"date":35,"type":20},{"date":64,"type":20},"2027-11",{"name":39,"class":40},{"id":67,"slug":68,"hasResults":11,"nctId":69,"briefTitle":70,"officialTitle":71,"acronym":72,"eligibilityCriteria":73,"healthyVolunteers":11,"sex":17,"minAge":74,"maxAge":4,"enrollmentInfo":75,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":77,"conditions":78,"keywords":81,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":83,"lastUpdatePostDateStruct":84,"startDateStruct":86,"completionDateStruct":88,"leadSponsor":90,"locationsCount":91},"100594281","the-sacral-erector-spinae-plane-block-in-total-knee-arthroplasty-100594281","NCT07017400","The Sacral Erector Spinae Plane Block in Total Knee Arthroplasty","Effectiveness of the Sacral Erector Spinae Plane (ESP) Block in Total Knee Arthroplasty: A Prospective Observational Study","sacral ESP","Inclusion Criteria:\n\n* Adults \\>18 years\n* ASA I-III\n* scheduled for unilateral TKA with expected hospitalization \\> 24 hours\n\nExclusion Criteria:\n\n* Refusal of consent\n* Local anesthetics allergies\n* contraindications to spinal or regional anesthesia\n* coagulation disorders\n* anticoagulation\u002Fantiaggregation medications\n* dementia\n* ASA-PS \\> III\n* ongoing infection\n* emergency surgeries","18 Years",{"count":76,"type":20},126,"The goal of this observational study is to learn about the analgesic efficacy and postoperative recovery of two locoregional anesthesia combinations in patients \\> 18 years (ASA I-III), scheduled for unilateral TKA under spinal anesthesia with expected hospitalization \\> 24 hours:\n\n* ACB + sacral ESP block\n* ACB + iPACK block\n\nThe main question it aims to answer is: Does the ACB + sacral ESP block combination produce effective postoperative recovery and analgesic effect?\n\nParticipants already taking ACB + sacral ESP block as part of their regular peri-operative care for TKA will be followed in the postoperative period for 48 hours.",[79,80],"Total Knee Anthroplasty","Regional Anesthesia",[57,82],"total knee arthroplasty","2025-08-22",{"date":85,"type":33},"2025-08-28",{"date":87,"type":33},"2025-07-16",{"date":89,"type":20},"2027-12",{"name":39,"class":40},1,""]