[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"pain-after-total-knee-arthroplasty\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:pain-after-total-knee-arthroplasty":48},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":10,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":28,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":5},"100640495",false,"NCT07629388","Combined Distal Femoral Nerve Block for Pain Control After Knee Replacement","Comparative Study Assessing the Efficacy of a Combined Distal Femoral Nerve Block for Postoperative Analgesia Following Total Knee Arthroplasty (TKA)","FEM-COMB","Inclusion Criteria:\n\n* Adult patients aged over 18 years.\n* Scheduled for total knee arthroplasty with multimodal analgesia.\n* Affiliated with or benefiting from a social security system.\n* Able to understand the study information and provide written informed consent.\n\nExclusion Criteria:\n\n* Emergency surgery.\n* Weight under 50 kg.\n* Body mass index over 40 kg\u002Fm².\n* Contraindication to nefopam, non-steroidal anti-inflammatory drugs, local anesthetics, or morphine.\n* Preoperative opioid use.\n* Antidepressant or gabapentinoid treatment.\n* Other planned surgical or medical procedures during the study period.\n* Participation in another clinical trial, or currently in an exclusion period from another trial.\n* Inability to understand study information for linguistic, psychological, cognitive, or literacy reasons.\n* Pregnancy, possible pregnancy without effective contraception, or breastfeeding.\n* Protected adults, including those under guardianship, curatorship, legal protection, detention, or otherwise unable to give informed consent.","ALL","18 Years",{"count":19,"type":20},240,"ESTIMATED","INTERVENTIONAL",[23],"NA","The goal of this clinical trial is to see whether a combined distal femoral nerve block improves pain relief after total knee replacement in adults having planned surgery. The main questions it aims to answer are:\n\n* Does the combined distal femoral nerve block reduce the amount of opioid needed in the post-anesthesia recovery room?\n* Does it preserve quadriceps muscle strength while improving postoperative pain control?\n\nResearchers will compare the combined distal femoral nerve block to a saphenous nerve block alone to see if the combined block provides better analgesia without reducing leg strength.\n\nParticipants will:\n\n* Receive either the combined distal femoral nerve block or the saphenous nerve block alone before surgery.\n* Also receive standard multimodal pain management, including anesthesia, surgical site infiltration, and postoperative pain medications.\n* Be assessed for pain, opioid use, nausea and vomiting, quadriceps strength, time to first standing, hospital stay length, and patient satisfaction from surgery until discharge.",[26,27],"Pain After Total Knee Arthroplasty","Pain Management",[29,30,31,32,33,34,35],"total knee arthroplasty","distal femoral nerve block","saphenous nerve block","femoral triangle block","postoperative pain","opioid consumption","regional anesthesia","NOT_YET_RECRUITING","2026-06-04",{"date":39,"type":40},"2026-06-05","ACTUAL",{"date":42,"type":20},"2026-05-25",{"date":44,"type":20},"2027-05-25",{"name":46,"class":47},"Ramsay Générale de Santé","OTHER",""]