[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"cardiac-complication\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:cardiac-complication":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,44],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":17,"targetDuration":20,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":28,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100301866","registry-for-the-improvement-of-postoperative-outcomes-in-cardiac-and-thoracic-surgery-100301866",false,"NCT03209674","Registry for the Improvement of Postoperative OutcomeS in Cardiac and Thoracic surgEry","RIPOSTE","Inclusion Criteria:\n\n* all patients eligible for cardiac or thoracic surgery\n\nExclusion Criteria:\n\n* non applicable","ALL",{"count":18,"type":19},8000,"ESTIMATED","2 Months","OBSERVATIONAL","The registry for the improvement of postoperative outcomes in cardiac and thoracic surgery aims to prospectively collect data in order to test the association between various preoperative and per-operative variables ; and several postoperative outcomes such as mortality, shock, redo surgery, sepsis and extracorporeal life-support.",[24,25,26,27],"Heart Diseases","Death","Postoperative Complications","Cardiac Complication",[29,30],"Cardiac surgery","Thoracic surgery","RECRUITING","2026-04-02",{"date":34,"type":35},"2026-04-03","ACTUAL",{"date":37,"type":35},"2012-01-01",{"date":39,"type":19},"2030-12-31",{"name":41,"class":42},"CMC Ambroise Paré","OTHER",1,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":4,"eligibilityCriteria":50,"healthyVolunteers":51,"sex":16,"minAge":4,"maxAge":52,"enrollmentInfo":53,"targetDuration":4,"studyType":55,"phases":56,"briefSummary":58,"conditions":59,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":43},"100597525","femoral-arterial-cannulation-in-pediatrics-100597525","NCT07059624","Femoral Arterial Cannulation in Pediatrics","Femoral Arterial Cannulation Performed by Anesthesia Residents: A Comparison Between Ultrasound-Guided \"Modified Dynamic Needle Tip Positioning, Short-Axis, Out-Of-Plane\" and \"Conventional, Short-Axis, Out-Of-Plane\" Methods","Inclusion Criteria:\n\n* Infants and children under 12 years of age.\n* American Society of Anesthesiologist (ASA) physical status II-IV.\n* Patients with congenital heart disease undergoing cardiac surgery who do not have existing arterial line access.\n\nExclusion Criteria:\n\n* Need for emergency surgery.\n* Hemodynamic instability.",true,"12 Years",{"count":54,"type":19},80,"INTERVENTIONAL",[57],"NA","The goal of this clinical trial\\] is to evaluate the efficacy and safety of the ultrasound-guided \"Modified Dynamic\n\nNeedle Tip Positioning Short-Axis, Out-Of-Plane\" (MDNTP-SAOP) technique compared to the \"Conventional, Short-Axis, Out-Of-Plane\" (C-SAOP) technique for femoral arterial cannulation performed by anesthesia residents in children. The main question it aims to answer is:\n\nWhat is the time required for attempted femoral arterial cannulation by anesthesia residents at the first puncture site?\n\nResearchers will compare the efficacy and safety of MDNTP-SAOP versus C-SAOP methods for femoral arterial cannulation performed by anesthesia residents in infants and children undergoing cardiac surgery.\n\nParticipants will be randomized to either the MDNTP-SAOP or the C-SAOP group. Intraoperatively, time taken for attempted cannulation by the resident at the first site of femoral arterial puncture, number of attempts at arterial cannulation, and number of cannulae required for successful cannula insertion will be recorded. Adverse events will be monitored on postoperative days 1 and 3. The insertion site will be examined for thrombosis, hematoma, infection, or limb ischemia distal to the insertion site",[60,27,61],"Pediatric ALL","Anesthesia","2025-07-18",{"date":64,"type":35},"2025-07-20",{"date":66,"type":35},"2025-07-09",{"date":68,"type":19},"2027-01-01",{"name":70,"class":42},"American University of Beirut Medical Center"]