[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"knee-replacement-arthroplasty\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:knee-replacement-arthroplasty":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,45,77],{"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":22,"briefSummary":24,"conditions":25,"keywords":28,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100593245","remote-monitoring-after-knee-replacement-surgery-100593245",false,"NCT07003932","Remote Monitoring After Knee Replacement Surgery","OA-AID TKR","Inclusion Criteria:\n\n* Men and women, 50 years of age or older\n* Referred to total or unicondylar knee replacement surgery due to knee osteoarthritis\n\nExclusion Criteria:\n\n* Revision of previous knee replacement surgery\n* Serious comorbidities (such as severe malignancies, severe diabetes mellitus, severe infections, uncontrollable hypertension, severe cardiovascular disease, severe respiratory disease)\n* Congitive dysfunction\n* Knee replacement surgery due to trauma or inflammatory joint disease (such as psoriatic arthritis or rheumatoid arthritis)\n* Unable to understand Norwegian\n* Low digital competency\u002F cannot answer questionnaires digitally (lack BankID, do not possess a smartphone)\n* Deemed inappropriate for remote monitoring by orthopedic surgeon","ALL","50 Years",{"count":19,"type":20},140,"ESTIMATED","INTERVENTIONAL",[23],"NA","The goal of this clinical trial is to evaluate the effect, cost-effectiveness, safety and satisfaction with replacing standardized, pre-scheduled face-to-face visits with remote monitoring and video consultations or face-to-face consultations only when needed after knee replacement surgery due to knee osteoarthritis.\n\nThe primary outcome is the probability of being a OMERACT-OARSI responder at 6 months post-surgery. This is a composite index where participants are classified as a responder or non-responder based on improvement in pain, function and\u002For disease activity. Health-related quality of life and healthcare costs will be used to determine cost-effectiveness. Patient-reported adverse events and statisfaction will be used to determine safety and satisfaction.\n\nPatients will be recruited from Diakonhjemmet Hospital. Patients undergoing knee replacement surgery will be randomly allocated to a control group who are summoned for a face-to-face consultation at Diakonhjemmet Hospital at 2 and 12 months, or a remote monitoring group who will not be scheduled for hospital visits but will answer patient-reported outcomes throught a web-application at 1, 2, 3, 6 and 12 months post-surgery and only be scheduled for hospital visits when needed.\n\nAn additional study with follow-up after 5 and 10 years will be conducted.",[26,27],"Knee Arthroplasty, Total","Knee Replacement Arthroplasty",[29,30,31],"knee arthroplasty","remote follow-up","non-inferiority","RECRUITING","2026-05-17",{"date":35,"type":36},"2026-05-19","ACTUAL",{"date":38,"type":36},"2025-06-04",{"date":40,"type":20},"2035-12-31",{"name":42,"class":43},"Diakonhjemmet Hospital","OTHER",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":51,"eligibilityCriteria":52,"healthyVolunteers":11,"sex":16,"minAge":53,"maxAge":4,"enrollmentInfo":54,"targetDuration":4,"studyType":21,"phases":56,"briefSummary":57,"conditions":58,"keywords":61,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":44},"100583759","comparing-articular-noise-and-its-perception-between-two-different-types-of-total-knee-arthroplasty-100583759","NCT06880497","Comparing Articular Noise and Its Perception Between Two Different Types of Total Knee Arthroplasty","Monocentric, Randomized Study, Comparing Articular Noise and Its Perception Between Two Different Types of Total Knee Arthroplasty","NATKA","Inclusion Criteria:\n\n* Adult patients receiving a primary TKA\n* Signed informed consent\n* Patients affiliated to a social security scheme\n* Patients willing and able to comply with study protocol requirements based on the investigator's judgment.\n\nExclusion Criteria:\n\n* History of knee surgery on the concerned\u002Fstudied knee (except arthroscopic surgery)\n* Patients presenting coronal deformities \\> 20°, varus laxity \\> 10° and\u002For valgus laxity \\> 15°\n* Patients receiving revision TKA\n* Pregnancy or breast-feeding\n* Patients with protected status under articles L1121-6, LL121-8 and L1122-2 of the French Public Health Code\n* Unable to comply with study procedures, based on the investigator's judgment.","18 Years",{"count":55,"type":20},170,[23],"Some patients complain of articular noise (such as clicking, snapping, cracking or popping) after a total knee replacement. Controversy remains about whether there is a correlation between articular noise and worse outcomes following a knee replacement. A study by Nam et al. on 1540 patients revealed an association between noise and residual symptoms 30 days after they received a total knee replacement. Conversely, a study by Kuriyama et al. on 60 patients revealed no correlation between noise and patient satisfaction after 1 year of receiving a total knee replacement. The incidence of noise following a knee replacement has rarely been studied as a primary outcome. Like pain, it could be considered an important patient-reported outcome to assess patient satisfaction. The study aims to compare the prevalence of patient-perceived noise of an ultra-congruent total knee prosthesis (Score 2, Amplitude) versus a posterior-stabilized total knee prosthesis (Anatomic, Amplitude).",[59,27,60],"Knee Osteoarthristis","Knee Replacement, Total",[62,63,64,65,66,67],"Noise","Articular noise","Total Knee Arthroplasty","TKA","Total Knee Replacement","TKR","2026-03-02",{"date":70,"type":36},"2026-03-04",{"date":72,"type":36},"2025-12-24",{"date":74,"type":20},"2028-12",{"name":76,"class":43},"Elsan",{"id":78,"slug":79,"hasResults":11,"nctId":80,"briefTitle":81,"officialTitle":82,"acronym":4,"eligibilityCriteria":83,"healthyVolunteers":84,"sex":16,"minAge":53,"maxAge":4,"enrollmentInfo":85,"targetDuration":4,"studyType":21,"phases":87,"briefSummary":88,"conditions":89,"keywords":92,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":96,"lastUpdatePostDateStruct":97,"startDateStruct":99,"completionDateStruct":101,"leadSponsor":103,"locationsCount":44},"100590494","investigating-patient-satisfaction-with-smart-knee-implants-100590494","NCT06968143","Investigating Patient Satisfaction With Smart Knee Implants","Evaluating the Impact of Remote Therapeutic Monitoring on Knee Arthroplasty Recovery","Inclusion Criteria:\n\n* Patients over 18 years of age\n* Patients undergoing unilateral primary or revision total knee arthroplasty with the smart knee implant or standard-of-care\n\nExclusion Criteria:\n\n* Patients who receive contralateral knee replacement or contralateral or unilateral hip replacement within 90 days before or after their knee replacement in this study\n* Patients with post-operative weight-bearing restrictions or physical deconditioning prohibiting routine physical therapy participation",true,{"count":86,"type":20},150,[23],"The main goal of this study is to see if there is a connection between the social and economic resources available in a patient's neighborhood (measured by the Area Deprivation Index, ADI) and their recovery after knee replacement surgery, as tracked through remote monitoring. A secondary goal is to find out if patients' self-reported pain and function score are linked to their actual physical improvement after surgery as measured by a remote therapeutic monitoring (RTM) device. Additionally, this study examines whether RTM can reduce the number of postoperative clinic visits within the first 90 days after surgery while maintaining patient satisfaction and patient-reported outcome measures (PROMs).",[64,90,27,91],"Knee Replacement","Knee Osteoarthritis",[93,64,94,95],"Smart Knee Implant","Remote Therapeutic Monitoring","Persona IQ","2025-12-15",{"date":98,"type":36},"2025-12-17",{"date":100,"type":36},"2025-09-01",{"date":102,"type":20},"2027-10-31",{"name":104,"class":43},"University of Chicago"]