[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Maxx Orthopedics Inc\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":65},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,43],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":17,"targetDuration":20,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":26,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":5},"100564324","prospective-in-vivo-post-market-safety-and-efficacy-surveillance-registry-of-the-maxx-orthopedics-freedom-total-knee-system-100564324",false,"NCT06627699","Prospective, In-Vivo, Post-Market Safety and Efficacy Surveillance Registry of the MAXX Orthopedics, Freedom Total Knee® System","INCLUSION CRITERIA:\n\nCandidates for this registry must meet ALL of the following criteria:\n\n* Patient is \\> 18 years of age\n* Patient has failed attempts at non-operative conservative therapy\n* Patient has participated in the informed consent process and signed an IRB approved informed consent\n* Patient is scheduled to undergo unilateral or bilateral primary TKA of the knee\n\nEXCLUSION CRITERIA:\n\nCandidates will be excluded from the evaluation if ANY of the following apply:\n\n* Patients with previous TKA, UKA, HTO or knee fusion of the indicated knee\n* Patients that have undergone previous surgery of indicated knee for tumor, trauma or fracture\n* Evidence of active or suspected (systemic or local) infection at time of surgery\n* Other significant disabling problems from the musculoskeletal system than in the knee (i.e.: muscular dystrophy, polio, neuropathic joints)\n* Patients with or having; malignancy - active malignancy, Paget's disease, renal osteodystrophy, immunologically suppressed, sickle cell anemia and systemic lupus erythematosus\n* Patients with neuromuscular or neurosensory deficit\n* Women who are pregnant\n* Prisoner or transient\n* Recent history of known narcotic abuse\n* Any significant psychological disturbance past or present, that could impair the consent process or ability to complete subject self-report questionnaires","ALL","18 Years",{"count":18,"type":19},300,"ESTIMATED","2 Years","OBSERVATIONAL","In an effort to satisfy regulatory requirements for post-market surveillance of product safety and efficacy, a representative sample of patients will be recruited for prospective monitoring.",[24,25],"Knee Osteoarthristis","Total Knee Anthroplasty",[27,28,29,30],"Registry","Primary TKA","Total Knee Arthroplasty","Total Knee Replacement","RECRUITING","2026-06-23",{"date":34,"type":35},"2026-06-26","ACTUAL",{"date":37,"type":35},"2025-11-01",{"date":39,"type":19},"2029-03-01",{"name":41,"class":42},"Maxx Orthopedics Inc","INDUSTRY",{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":4,"eligibilityCriteria":49,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":50,"targetDuration":4,"studyType":52,"phases":53,"briefSummary":55,"conditions":56,"keywords":58,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":60,"startDateStruct":61,"completionDateStruct":63,"leadSponsor":64,"locationsCount":5},"100564322","multicenter-ide-study-of-the-peek-optima-femoral-component-vs-a-cocr-alloy-tka-femoral-component-of-similar-design-100564322","NCT06627673","MultiCenter IDE Study of the PEEK-OPTIMA™ Femoral Component vs a CoCr Alloy TKA Femoral Component of Similar Design","MultiCenter Prospective Parallel Registry Controlled Investigational Device Exemption Clinical Study to Determine Non-Inferiority of the PEEK-OPTIMA™ Femoral Component Versus a CoCr Alloy Femoral Component of Similar Design for TKA","Inclusion Criteria:\n\n* Male and female subjects 18 years of age or older.\n* Subjects with a primary diagnosis of end-stage symptomatic unilateral primary knee osteoarthritis.\n* Subjects with a pre-operative Knee Society Score (KSS) Knee score of \\>25 and \\\u003C75.\n* Subjects who, in the opinion of the Investigator, can understand this clinical investigation, co-operate with the investigational procedures and are willing to return to the hospital for all the required post-operative follow-ups.\n* Subjects who can give voluntary, written informed consent to participate in this clinical investigation and from whom consent has been obtained.\n\nExclusion Criteria:\n\n* Subjects who, in the opinion of the Investigator, have an existing condition that would compromise their participation and follow-up in this clinical investigation.\n* Subjects who are known drug or alcohol abusers or with psychological disorders that could affect follow-up care or treatment outcomes.\n* Subjects who have participated in a clinical study with an investigational product in the last 6 months.\n* Subjects with other significant disabling problems from the muscular-skeletal system other than in the knees (i.e.: muscular dystrophy, polio, neuropathic joints).\n* Subjects with known osteoporosis and\u002For previous history of fracture related to osteoporosis.\n* Subjects with a current or active history of malignancy, active or suspected infection, Paget's disease, renal osteodystrophy, immunologically suppressed, rheumatoid arthritis, sickle cell anemia, and systemic lupus erythematosus.\n* Subjects defined by the Investigator as American Society of Anesthesiologists (ASA) Grade III or IV.\n* Subjects who have a neuromuscular or neurosensory deficit.\n* Female subjects who are pregnant or lactating.\n* Subjects with an anatomical limb alignment of above 20 degrees varus or valgus.\n* Subjects with primary or secondary diagnosis of inflammatory or traumatic arthritis.\n* Subjects with a fixed flexion deformity of over 20 degrees.\n* Subjects with recurvatum (definition: hyperextension ≥ 5 degrees).\n* Subjects who have previously undergone surgery on the indicated knee including total knee arthroplasty, patellofemoral arthroplasty, or unicondylar knee arthroplasty, high tibial osteotomy, ligament reconstruction, fusion, open reduction and internal fixation.\n* Subjects that have undergone, or scheduled to undergo, contralateral total knee arthroplasty or unicondylar knee arthroplasty within ±1 year from the study surgical procedure.\n* Evidence of active or suspected (systemic or local) infection at time of surgery.",{"count":51,"type":19},200,"INTERVENTIONAL",[54],"NA","The purpose of this investigational device exemption (IDE) study is to monitor the performance (safety and efficacy) of the Maxx Orthopedics, Freedom Total Knee® System, with a femoral component of similar design, manufactured from polyether-ether-ketone (PEEK).",[57],"Knee Osteoarthritis",[30,29,59],"Polyether-ether-ketone",{"date":34,"type":35},{"date":62,"type":35},"2026-01-01",{"date":39,"type":19},{"name":41,"class":42},""]