[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100553580":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":20,"centralContacts":25,"locations":34,"responsibleParty":49,"collaborators":10,"id":51,"slug":10,"hasResults":52,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":56,"eligibilityCriteria":57,"healthyVolunteers":52,"sex":58,"minAge":59,"maxAge":10,"enrollmentInfo":60,"targetDuration":63,"studyType":64,"phases":10,"briefSummary":65,"conditions":66,"keywords":10,"overallStatus":36,"whyStopped":10,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":78},{"fullName":5,"class":6},"CornerLoc","INDUSTRY",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Implanted TransLoc 3D SIJ Fusion Patients",null,"Patients who were diagnosed with sacroiliitis and were treated with the TransLoc 3D System ≥ 1 year ≤ 18 months at the time of consent.",[13],"Device: TransLoc 3D SI Joint Fusion System",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":10},"DEVICE","TransLoc 3D SI Joint Fusion System","Satisfaction survey will be administered to collect real world evidence on patients that previously received the TransLoc 3D System commercially.",[9],[21],{"name":22,"affiliation":23,"role":24},"Lee James, DO","Advanced Orthopedic Center","PRINCIPAL_INVESTIGATOR",[26,31],{"name":27,"role":28,"phone":29,"phoneExt":10,"email":30},"Carley Wiegner","CONTACT","888-743-8736","carley@cornerloc.com",{"name":32,"role":28,"phone":10,"phoneExt":10,"email":33},"Bob Compton","bob@cornerloc.com",[35],{"facility":23,"status":36,"city":37,"state":38,"zip":39,"country":40,"cosmosGeoPoint":41,"geoPoint":46,"contacts":47},"RECRUITING","Port Charlotte","Florida","33948","United States",{"type":42,"coordinates":43},"Point",[44,45],-82.09064,26.97617,{"lat":45,"lon":44},[48],{"name":22,"role":28,"phone":10,"phoneExt":10,"email":10},{"type":50,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR","100553580",false,"NCT06487936","Real-World Registry Study on Patient Satisfaction With TransLoc 3D SI Joint Fusion","A Multi-Center, Real World Prospective\u002FRetrospective Registry to Evaluate Patient Satisfaction With the TransLoc 3D SI Joint Fusion System","RELIEF","Inclusion Criteria:\n\n* Age 18 year or older\n* Confirmed Implant of the Transloc 3D Fusion System\n* Did not have Transloc device removed or another manufacturer device implanted post Transloc\n* Does not have other manufacturer's titanium or metal implant\n* Patient may be included with prior allograft implant\n* Willing to participate and give written consent\n* Must have or planned CT post ≥1 year per standard of care\n\nExclusion Criteria:\n\n* Patient is younger than 18 years\n* Patient is unable to sign the Informed Consent\n* Implant of other manufacturer's titanium or alternative metal implant\n* Revision with another manufacturer's implant\n* Fracture or unresolved trauma of implant side after implantation of TransLoc\n* Patient unwilling to participate in Patient Satisfaction Survey\n* Patient has not returned for Standard of Care follow-up","ALL","18 Years",{"count":61,"type":62},120,"ESTIMATED","18 Months","OBSERVATIONAL","This is a multi-center, consecutive enrollment registry study to evaluate patient satisfaction post SI Fusion with the TransLoc 3D SI Fusion System.",[67,68],"Sacroiliac Joint Dysfunction","Sacroiliac; Fusion","2024-08-21",{"date":71,"type":72},"2024-08-23","ACTUAL",{"date":74,"type":72},"2024-08-15",{"date":76,"type":62},"2024-12-15",{"name":5,"class":6},1]