[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Restor3D\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":45},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"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":21,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":27,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":4},"100636293","the-restor3d-outcomes-registry-100636293",false,"NCT07563803","The restor3d Outcomes Registry","The restor3d Outcomes Registry: Tracking Patient Recovery After Joint Replacement","Master Protocol Inclusion Criteria:\n\n* Age ≥ 18 years\n* Prescribed an FDA-cleared or approved orthopedic implant manufactured by restor3d, Inc.\n\nMaster Protocol Exclusion Criteria:\n\n* Patient is receiving an implant not manufactured by restor3d\n* Patient is receiving a restor3d implant that is not FDA-cleared or approved\n* Patient lives outside the United States\n* Patient is receiving a restor3d implant that does not use a patient-specific plan, instrumentation or implant\n* Patient is non-English-speaking\n* Patient is receiving a restor3d implant outside of the defined implant cohorts\n* Patient does not provide informed consent\n* Plus additional cohort-specific exclusion criteria","ALL","18 Years",{"count":19,"type":20},2000,"ESTIMATED","5 Years","OBSERVATIONAL","The restor3d Outcomes Registry is a prospective, longitudinal, decentralized study designed to capture patient-reported outcomes (PROs) from adults who have received an FDA-cleared or approved restor3d patient-specific orthopedic implant. Using a master protocol framework, the study enrolls patients across multiple joint cohorts (knee, hip, foot \\& ankle, shoulder) under a single protocol, with joint-specific details governed by individual appendices. Participants self-enroll and complete electronic PRO surveys (ePROs) before surgery and at 6 weeks, 3 months, 6 months, and annually through 5 years post-operatively, all remotely, with no required in-person visits. The study aims to quantify changes in pain, function, quality of life, and satisfaction over time, and to establish real-world outcome benchmarks for patient-specific orthopedic implants.",[25,26],"Joint Replacement","Arthropathy",[28,29,30,31,32],"Knee arthroplasty","Hip arthroplasty","Ankle arthroplasty","Shoulder arthroplasty","restor3d","NOT_YET_RECRUITING","2026-04-30",{"date":36,"type":37},"2026-05-04","ACTUAL",{"date":39,"type":20},"2026-05-31",{"date":41,"type":20},"2032-05-31",{"name":43,"class":44},"Restor3D","INDUSTRY",""]