[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"gonarthritis\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:gonarthritis":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,45],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":24,"conditions":25,"keywords":28,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100566597","clinical-performance-and-safety-of-the-unicompartmental-univation-xf-pro-implant-100566597",false,"NCT06657248","Clinical Performance and Safety of the Unicompartmental Univation® XF Pro Implant","Prospective, Multicenter Study Evaluating the Midterm Clinical Performance and Safety of the Unicompartmental Univation® XF Pro Knee Implant","UNI_XF_PRO","Inclusion Criteria:\n\n* Indication for a primary medial unicompartmental knee endoprosthesis\n\nAcc. to Instructions for Use:\n\n* Both cruciate ligaments intact\n* Lateral ligaments intact\n* Leg axis amenable to passive correction\n* Varus deformity under 15°\n* Bending capability of at least 90°\n* Extension deficit no greater than 5-10°\n* Written informed consent of patient\n* Kellgran \\& Lawrence Score \\> II (only straight or varus\n* Patients with moderate radiological symptoms\n* Patients without clinical symptoms\n\nExclusion Criteria:\n\n* Pregnancy\n* Patient age \\\u003C18 and \\> 75 years\n* BMI ≥ 40\n* High risk patients ASA \\> III","ALL","18 Years","75 Years",{"count":21,"type":22},150,"ESTIMATED","OBSERVATIONAL","The study is designed as a prospective, observational, mid-term, multi-center follow-up study. It is planned to include 150 patients from 4 different study centres in Germany.",[26,27],"Gonarthritis","Degenerative Disease",[29,30,31],"Degenerative medial unicompartmental Gonarthrosis","Unicompartmental knee arthroplasty","Safety and Performance","RECRUITING","2026-05-05",{"date":35,"type":36},"2026-05-08","ACTUAL",{"date":38,"type":36},"2026-04-02",{"date":40,"type":22},"2032-10",{"name":42,"class":43},"Aesculap AG","INDUSTRY",4,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":51,"eligibilityCriteria":52,"healthyVolunteers":53,"sex":54,"minAge":55,"maxAge":56,"enrollmentInfo":57,"targetDuration":4,"studyType":59,"phases":60,"briefSummary":62,"conditions":63,"keywords":67,"overallStatus":72,"whyStopped":4,"lastUpdateSubmitDate":73,"lastUpdatePostDateStruct":74,"startDateStruct":76,"completionDateStruct":78,"leadSponsor":80,"locationsCount":4},"100590804","proprioceptive-fatigue-adaptation-in-osteoarthritis-100590804","NCT06972186","Proprioceptive Fatigue Adaptation in Osteoarthritis","Neuromotor Adaptation to Fatigue: Changes in Lower Extremity Proprioception in Patients With Osteoarthritis","PROFA-OA","Inclusion Criteria:\n\n* Female, aged 50-65\n* Postmenopausal\n* Grade 2-3 knee osteoarthritis (Kellgren-Lawrence Scale) for OA group\n* No lower extremity surgery in the last 6 months\n* No neuromuscular or orthopedic condition affecting the lower extremities\n\nExclusion Criteria:\n\n* Severe balance disorders or vestibular disease\n* Bilateral knee prosthesis or severe osteoporosis\n* Lower extremity musculoskeletal injury in the last 6 months",true,"FEMALE","45 Years","65 Years",{"count":58,"type":22},20,"INTERVENTIONAL",[61],"NA","This study aims to investigate the effects of fatigue induced by isokinetic exercise on passive and active joint position sense in postmenopausal women diagnosed with knee osteoarthritis (gonarthrosis). A healthy control group matched for age and sex will also be included for comparative analysis. Participants will undergo proprioceptive assessments before and after an isokinetic fatigue protocol. We hypothesize that (1) fatigue will impair both passive and active joint position sense in patients with gonarthrosis, (2) active joint position sense will be more affected than passive sense, and (3) the deterioration in proprioception will be greater in the gonarthrosis group compared to healthy controls.",[64,65,66,26],"Osteoarthritis of Knee","Proprioception","Isokinetic Test",[68,69,70,71],"osteoarthritis of knee","propripception","isokinetic test","gonarthritis","NOT_YET_RECRUITING","2025-05-06",{"date":75,"type":36},"2025-05-14",{"date":77,"type":22},"2025-06-01",{"date":79,"type":22},"2025-12-01",{"name":81,"class":82},"Kocaeli Sağlık ve Teknoloji Üniversitesi","OTHER"]