[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"complication-of-anesthesia\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:complication-of-anesthesia":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,50],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":30,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":49},"100454296","acute-acute-surgical-care--risk-factors-and-outcomes-for-patients-in-need-of-acute-surgical-care-100454296",false,"NCT05195697","ACUTE-Acute Surgical Care- Risk Factors and Outcomes for Patients in Need of Acute Surgical Care","ACUTE","Inclusion Criteria: Patients admitted to Skåne University hospital in need of acute surgical care -\n\nExclusion Criteria: Below 18 years old\n\n\\-","ALL","18 Years",{"count":19,"type":20},3000,"ESTIMATED","OBSERVATIONAL","Observational retrospective study of patients in need of acute surgical care admitted to Skåne University Hospital between 2009 and 2019.",[24,25,26,27,28,29],"Risk Factors","Complication of Surgical Procedure","Complication of Treatment","Complication of Anesthesia","Long Term Effects After Emergency Surgery","Long Term Effects After GI Bleeding",[31,32,33,34,35,36],"Emergency surgery","Acute surgery","Complications","Risk factors","Frailty","Ageing","RECRUITING","2026-06-15",{"date":40,"type":41},"2026-06-17","ACTUAL",{"date":43,"type":41},"2020-01-01",{"date":45,"type":20},"2030-12",{"name":47,"class":48},"Region Skane","OTHER",1,{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":56,"eligibilityCriteria":57,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":58,"targetDuration":4,"studyType":60,"phases":61,"briefSummary":63,"conditions":64,"keywords":71,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":75,"lastUpdatePostDateStruct":76,"startDateStruct":78,"completionDateStruct":80,"leadSponsor":82,"locationsCount":49},"100614824","pericapsular-nerve-group-peng-block-combined-with-lateral-femoral-cutaneous-nerve-lfcn-block-or-wound-infiltration-for-postoperative-analgesia-in-anterior-approach-total-hip-arthroplasty-a-randomized-controlled-trial-100614824","NCT07284615","Pericapsular Nerve Group (PENG) Block Combined With Lateral Femoral Cutaneous Nerve (LFCN) Block or Wound Infiltration for Postoperative Analgesia in Anterior Approach Total Hip Arthroplasty: A Randomized Controlled Trial","Lateral Femoral Cutaneous Nerve (LFCN) Block or Wound Infiltration (WI) Combined With Pericapsular Nerve Group (PENG) Block for Analgesia in Elective Anterior Approach Total Hip Arthroplasty: A Randomized Controlled Trial","Peng_lfcn\u002FWI","Inclusion Criteria:\n\n* Age \\> 18 years\n* Elective total hip arthroplasty\n* Spinal (subarachnoid) anesthesia\n* Written informed consent provided by the patient or by the legal guardian, if appointed\n\nExclusion Criteria:\n\n* INR \\> 1.5\n* aPTT \\> 1.5\n* Platelet count \\\u003C 75,000\u002Fmm³\n* Signs suggestive of infection at the puncture site\n* Absence of informed consent to the procedure\n* Documented or suspected allergy to local anesthetics",{"count":59,"type":20},102,"INTERVENTIONAL",[62],"NA","This prospective, randomized controlled trial aims to compare two multimodal regional anesthesia strategies for postoperative analgesia in elective total hip arthroplasty (THA) performed via anterior approach. Patients will be randomized to receive either a Pericapsular Nerve Group (PENG) block combined with a Lateral Femoral Cutaneous Nerve (LFCN) block, or a PENG block combined with wound infiltration (WI).\n\nThe primary outcome is postoperative pain intensity at rest, measured by Numerical Rating Scale (NRS) at 6 hours after surgery. Secondary outcomes include dynamic pain scores at 6, 24, and 48 hours, total opioid consumption, time to first rescue analgesia, quadriceps strength, hip flexion angle, length of stay, and adverse events.\n\nAll procedures are routinely used in clinical practice and carry minimal additional risk. Safety will be continuously monitored by the Principal Investigator and the study team according to an internal Safety Monitoring Plan.",[65,66,67,27,68,69,70],"Arthropathy of Hip","Hip Arthropathy","Locoregional Anesthesia","Regional Anesthesia Morbidity","Hospital Stay, Length of Stay in Hospital From Time of Surgery Till Discharge","Opioid Consumption",[72,73,74],"Postoperative muscle weakness","ERAS","Regional Block","2026-03-21",{"date":77,"type":41},"2026-03-25",{"date":79,"type":41},"2026-01-26",{"date":81,"type":20},"2026-11",{"name":83,"class":48},"Ospedale Edoardo Bassini"]