[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Materialise\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":62},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,39],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":25,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":28,"lastUpdatePostDateStruct":29,"startDateStruct":32,"completionDateStruct":34,"leadSponsor":36,"locationsCount":5},"100586027","long-term-safety-and-performance-of-cmf-porous-titanium-implants-100586027",false,"NCT06910033","Long-term Safety and Performance of CMF Porous Titanium Implants","CMF SafeTi Fit: Long-term Safety and Performance of CMF Porous Titanium Implants","CMF SafeTi Fit","Inclusion Criteria:\n\n* Age: Patients of any age are eligible for this study.\n* Patients treated with Materialise patient-specific CMF Porous Titanium Implants for facial and\u002For cranial reconstruction.\n* Patients who have followed Standard of Care, as determined in each case by the treating surgeon.\n\nExclusion Criteria:\n\n* Known hypersensitivity to Titanium at the time of surgery.\n* Patients who had or will receive the TMJ Total Arthroplasty System.\n* Pregnancy at the time of surgery.","ALL",{"count":19,"type":20},200,"ESTIMATED","OBSERVATIONAL","The goal of this retrospective study is to evaluate the clinical characteristics, efficiency, safety, and long-term performance of craniomaxillofacial (CMF) Porous Titanium Implants within the standard of care across children (0 - \\\u003C12 years old), adolescent (12 - \\\u003C22 years old), and adult (≥ 22 years old) populations.",[24],"Craniofacial Defects",[24,26],"Implants","NOT_YET_RECRUITING","2025-09-26",{"date":30,"type":31},"2025-09-29","ACTUAL",{"date":33,"type":20},"2025-11",{"date":35,"type":20},"2026-11",{"name":37,"class":38},"Materialise","INDUSTRY",{"id":40,"slug":41,"hasResults":11,"nctId":42,"briefTitle":43,"officialTitle":44,"acronym":4,"eligibilityCriteria":45,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":46,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":48,"conditions":49,"keywords":51,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":53,"lastUpdatePostDateStruct":54,"startDateStruct":56,"completionDateStruct":58,"leadSponsor":60,"locationsCount":61},"100589189","long-term-safety-and-performance-of-materialises-patient-specific-tmj-system-100589189","NCT06951178","Long-term Safety and Performance of Materialise's Patient-specific TMJ System.","Unlocking TMJs Clinical Study: Safety and Performance of Materialise's Patient-specific TMJ System","Inclusion Criteria:\n\n* Patients prescribed with Materialise TMJ Total Arthroplasty System for TMJ reconstruction\n* Patient who has received and understood the study information leaflet and has agreed to participate in the study and signed the informed consent form (ICF) (adult or legal guardian(s) if minor).\n\nExclusion Criteria:\n\n* Known hypersensitivity to Titanium, Nickel, or Cobalt-Chrome alloys.\n* Patient conditions where there is not enough bone quality or quantity to support the components.\n* Active infection in the anatomical area or the vicinity of the site to be implanted, preventing the implantation of the device.\n* Patients with marked hyperfunctional habits (e.g., tooth clenching, bruxism).\n* Pregnant woman.\n* Patient is known to be or suspected of being unable to comply with the study protocol or proposed follow-up visits by the investigator.",{"count":47,"type":20},30,"This is a long-term (10 years), retrospective-prospective, observational, single-arm, monocenter study of patients to be treated with the Materialise TMJ Total Arthroplasty System for TMJ replacement. The study will evaluate the efficiency, safety, clinical performance, accuracy, benefits, and risks associated with long-term use and the impact on life quality and diet of the TMJ system, its fixation devices, TMJ Implant trial, and guides in the adolescent and adult populations.",[50],"Temporomandibular Joint Disorders",[50,52],"Implant","2025-04-22",{"date":55,"type":31},"2025-04-30",{"date":57,"type":20},"2025-06",{"date":59,"type":20},"2037-06",{"name":37,"class":38},1,""]