[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"periprosthetic-fractures\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:periprosthetic-fractures":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,48,73],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":30,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100641087","post-market-clinical-follow-up-pmcf-study-evaluating-the-safety-and-efficacy-of-tpmed-revision-hip-prosthesis-system-100641087",false,"NCT07653295","Post-Market Clinical Follow-Up (PMCF) Study Evaluating the Safety and Efficacy of Tıpmed™ Revision Hip Prosthesis System","A Multicenter, Prospective, Observational, Post-Market Clinical Follow-Up (PMCF) Study Evaluating the Safety and Efficacy of Tıpmed™ Revision Hip Prosthesis System","Inclusion Criteria:\n\n* Individuals aged 18 years and older,\n* Male or female participants,\n* Participants who have undergone Revision Hip Arthroplasty (either total revision or partial component revision) for any indication (such as a documented joint failure or prosthesis-related clinical complication),\n* Participants in whose revision procedure the Tıpmed™ Revision Hip Prosthesis System components were utilized,\n* Participants who are not legally restricted (e.g., military personnel, convicts, or individuals under legal guardianship),\n* Participants who have voluntarily signed the written Informed Consent Form (ICF).\n\nExclusion Criteria:\n\n* Subjects currently participating in any other interventional clinical trial.","ALL","18 Years",{"count":19,"type":20},35,"ESTIMATED","OBSERVATIONAL","This is a multicenter, prospective, observational, post-market clinical follow-up (PMCF) study designed to evaluate the safety and clinical performance of the Tipmed™ Revision Hip Prosthesis System in adult participants undergoing revision hip arthroplasty. The study aims to gather real-world clinical evidence on the 24-month post-operative safety profile, potential complications, and functional outcomes of the device during routine clinical practice.",[24,25,26,27,28,29],"Revision Hip Arthroplasty","Aseptic Loosening of Prosthetic Joint","Prostheses-related Infections","Joint Instability","Periprosthetic Fractures","Prosthesis Failure",[31,24,32,33,34],"Hip Prosthesis","Revision Hip Prosthesis","Post-Market Clinical Follow-Up (PMCF)","Harris Hip Score (HHS)","RECRUITING","2026-06-17",{"date":38,"type":39},"2026-06-18","ACTUAL",{"date":41,"type":39},"2024-03-12",{"date":43,"type":20},"2029-03-31",{"name":45,"class":46},"TIPMED Medical Device Manufacturing Ltd. Co.","INDUSTRY",4,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":54,"eligibilityCriteria":55,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":56,"targetDuration":58,"studyType":21,"phases":4,"briefSummary":59,"conditions":60,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":72},"100314825","periprosthetic-fracture-registry-ppfx-100314825","NCT03378557","Periprosthetic Fracture Registry (PPFx)","Multicenter Prospective Registry for Periprosthetic Fractures After Hip or Knee Arthroplasty","PPFx","Inclusion Criteria:\n\n* Age ≥18 years\n\n  * Post-operative PPFx after total or hemi hip or total or unicondylar knee arthroplasty (including the acetabulum, femur, patella and proximal tibia) requiring\n\n    * osteosynthesis alone or\n    * component revision plus plate\u002Fnail osteosynthesis\n  * Informed consent obtained, i.e.:\n\n    * Ability of the patient or assigned representative to understand the content of the patient information \u002F Informed Consent Form\n    * Signed and dated EC \u002F IRB approved written informed consent\n  * Ability to attend post-operative follow up visits\n\nExclusion Criteria:\n\n* Pregnancy or women planning to conceive within the study period\n* Prisoner",{"count":57,"type":20},600,"12 Months","This registry supports international data collection and research on PPFx treatments after hip and knee arthroplasty.\n\nA registry such as this ultimately aims to provide far-reaching benefits to society including reduced morbidity and mortality, improved patient safety, improved quality of care and medical decision-making, reduced medical spending, and advances in orthopaedic science.",[28,61],"Periprosthetic Fracture Around Prosthetic Joint Implant","2025-09-08",{"date":64,"type":39},"2025-09-12",{"date":66,"type":39},"2018-12-31",{"date":68,"type":20},"2027-03-31",{"name":70,"class":71},"AO Innovation Translation Center","OTHER",13,{"id":74,"slug":75,"hasResults":11,"nctId":76,"briefTitle":77,"officialTitle":78,"acronym":79,"eligibilityCriteria":80,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":81,"targetDuration":83,"studyType":21,"phases":4,"briefSummary":84,"conditions":85,"keywords":89,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":101,"lastUpdatePostDateStruct":102,"startDateStruct":104,"completionDateStruct":106,"leadSponsor":108,"locationsCount":110},"100413461","peri-implant-and-peri-prosthetic-fractures-epidemiology-morbidity-mortality-treatment-and-outcome-analysis-100413461","NCT04663893","Peri-Implant and Peri-Prosthetic Fractures: Epidemiology, Morbidity, Mortality, Treatment and Outcome Analysis","Peri-Implant and Peri-Prosthetic Fractures: Epidemiology, Morbility, Mortality, Treatment and Functional Outcome Analysis. A Prospective Multi Center Observational Collaborative Study","PIPPAS","Inclusion Criteria:\n\n* Patient with the diagnose of Periprosthetic fracture of the shoulder, elbow, hip or knee. Or patients with the diagnose of Peri-implant fracture of the scapula, humerus, forearm, pelvis, femur, patella, tibia or fibula. Or patient presenting cut-out or cut-in after DHS or nail after a proximal humeral fracture.\n* 18 years or older\n\nExclusion Criteria:\n\n* Spine PP or PI fracture\n* PP or PI secondary to metastasis or tumoral fracture\n* PP or PI intraoperative fracture\n* PP or PI pathologic fracture\n* PP ankle fracture\n* PP or PI wrist or hand fracture\n* Fixation failure without any new fracture line: except cut-out or cut-in after DHS or nail of a proximal humeral fracture.\n* Pregnancy",{"count":82,"type":20},2500,"5 Years","This study supports Spanish data collection and analysis on Periprosthetic and Peri-implant fractures of the upper and lower limb. Treatment and clinical management of this fractures are complex and goes along with complications. There will be more than 70 hospitals providing information. This study will provide evidence on which is the best treatment for every unique patient. This will help trauma surgeons and geriatricians to provide better treatments, to improve health care in our society, reducing mortality, morbidity, improving functional outcomes, and reducing costs, which in turn will be advances in trauma care.",[86,87,28,88],"Periprosthetic Fracture of the Upper or Lower Limb","Peri-implant Fracture of the Upper or Lower Limb","Peri-implant Fracture",[90,91,92,93,94,95,96,97,98,99,100],"Periprosthetic fracture","peri-implant fracture","mortality","morbidity","loosening","prosthesis revision","fixation","osteosynthesis","complication","ambulate","quality of life","2022-01-16",{"date":103,"type":39},"2022-02-01",{"date":105,"type":39},"2021-01-01",{"date":107,"type":20},"2027-12-31",{"name":109,"class":71},"Hospital Clínico Universitario de Valladolid",7]