[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"posttraumatic-arthropathy\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:posttraumatic-arthropathy":101},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,48,77],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":10,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":29,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100514587",false,"NCT05980442","Comparative Study of Navigation-assisted OrthoPilot® Elite and Robotic-assisted MAKO® Total Knee Arthroplasty","Randomized, Controlled, Single Center Observational Study to Compare the Safety and Performance of Navigation-assisted OrthoPilot® Elite and Robotic-assisted MAKO® Total Knee Arthroplasty","ORMAK","Inclusion Criteria:\n\n* Indication for a TKA with a fixed-bearing total knee endoprosthesis\n* Written informed consent for participating in the clinical study\n\nExclusion Criteria:\n\n* Patient age \\\u003C18 years and \\>90 years\n* Patient not willing to participate at the follow-up\n* Pregnancy\n* retropatellar arthrosis requiring patella resurfacing\n* American Society of Anaesthesiologists (ASA) Classification \\>3","ALL","18 Years","90 Years",{"count":20,"type":21},140,"ESTIMATED","OBSERVATIONAL","Randomized, controlled, single center observational study to compare the safety and performance of navigation-assisted OrthoPilot Elite and robotic-assisted MAKO total knee arthroplasty (TKA). The aim of the study is the comparison of the clinical outcome between navigated and robotic-assisted TKA. The hypothesis of the study is that both treatments achieve similar results regarding functional and clinical aspects.",[25,26,27,28],"Osteoarthritis, Knee","Joint Diseases","Rheumatoid Arthritis of Knee","Posttraumatic Arthropathy",[30,31,32,33,34],"computer assisted orthopedic surgery","robotic assisted orthopedic surgery","orthopedic navigation","total knee arthroplasty","total knee replacement","RECRUITING","2026-03-26",{"date":38,"type":39},"2026-03-27","ACTUAL",{"date":41,"type":39},"2024-07-03",{"date":43,"type":21},"2028-12",{"name":45,"class":46},"Aesculap AG","INDUSTRY",1,{"id":49,"slug":4,"hasResults":10,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":53,"eligibilityCriteria":54,"healthyVolunteers":10,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":55,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":57,"conditions":58,"keywords":64,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":76},"100462536","NCT05302934","Evaluation of the PHENO4U Data Platform in Patients Undergoing Total Knee Arthroplasty","Prospective, Multinational Pilot Study for Evaluation of the PHENO4U Data Platform in Total Knee Arthroplasty Patients","Pheno4U Pilot","Inclusion Criteria:\n\n* Patient undergoing a total knee arthroplasty with a B. Braun knee implant system\n* Signed written informed consent\n* Patient's willingness \\& ability to use the \"BPMpathway\"sensor\n* Patient's willingness \\& ability to use the \"4Patient\" application\n\nExclusion Criteria:\n\n* Patient age \\\u003C 18 years\n* Patient not willing to participate at the further follow-up\n* Pregnancy\n* If intraoperatively an implant from a different manufacturer is used, the study patient has to be excluded from the study.",{"count":56,"type":21},600,"Prospective, multinational pilot study for evaluation of the Pheno4U data platform in Total Knee Arthroplasty (TKA) patients",[59,60,28,61,62,63],"Degenerative Osteoarthritis","Rheumatoid Arthritis","Chronic Instability of Knee","Stiffness of Knee","Deformity Knee",[65,66,67],"bi-condylar knee replacement","severe knee joint conditions","patient reported outcome","2026-02-24",{"date":70,"type":39},"2026-02-27",{"date":72,"type":39},"2022-09-28",{"date":74,"type":21},"2028-03",{"name":45,"class":46},4,{"id":78,"slug":4,"hasResults":10,"nctId":79,"briefTitle":80,"officialTitle":81,"acronym":82,"eligibilityCriteria":83,"healthyVolunteers":10,"sex":16,"minAge":17,"maxAge":84,"enrollmentInfo":85,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":87,"conditions":88,"keywords":89,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":93,"lastUpdatePostDateStruct":94,"startDateStruct":96,"completionDateStruct":98,"leadSponsor":100,"locationsCount":76},"100589520","NCT06955481","Study to Evaluate the Performance of Navigated TKA With OrthoPilot® pheno4u TKA Level 1","Prospective, Single-arm, Multicenter Study to Evaluate the Performance of Navigated Total Knee Arthroplasty Using the OrthoPilot and the Software pheno4u TKA Level 1","TKA4U","Inclusion Criteria:\n\n* Indication for a TKA with the OrthoPilot® Navigation System with a Aesculap total knee endo-prosthesis\n* Written signed informed consent of patient\n* Willingness and mental ability to participate at the long-term follow-up examinations\n\nExclusion Criteria:\n\n* Pregnancy\n* Patients \\\u003C 18 years or \\> 80 years\n* Patients unable to participate at the follow-up examination (physically, mentally)\n* Previous joint replacement at the index knee\n* ASA classification \\> 3 ( ASA I: A healthy patient without systemic diseases. ASA II: A patient with a mild systemic disease that is well controlled (e.g., well-controlled diabetes or hypertension). ASA III: A patient with a severe systemic disease that causes functional limitations (e.g., poorly controlled diabetes, COPD). ASA IV: A patient with a life-threatening systemic disease (e.g., severe heart failure, sepsis). ASA V: A dying patient who is not expected to survive without the operation. ASA VI: A deceased patient whose organs are being removed for donation.)","80 Years",{"count":86,"type":21},120,"The purpose of this PMCF study is to demonstrate the accuracy of navigation using the new pheno4uTKA Level 1 software for OrthoPilot Elite® and to evaluate its safety and performance.\n\nPatient-related outcome measures (PROM) will be acquired to investigate functional outcome and patient satisfaction.",[25,26,27,28],[90,91,92],"Navigation","Total Knee Arthroplasty","OrthoPilot","2025-11-14",{"date":95,"type":39},"2025-11-17",{"date":97,"type":39},"2025-10-07",{"date":99,"type":21},"2028-06",{"name":45,"class":46},""]