[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"sacroiliac-fusion\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:sacroiliac-fusion":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,46,74,104],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"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":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":4},"100633731","real-world-evidence-of-si-bones-ifuse-torq-tnt-advancing-treatment-of-pelvic-ring-fractures-100633731",false,"NCT07530497","Real World Evidence of SI-BONE's iFuse TORQ TNT Advancing Treatment of Pelvic Ring Fractures","REBAR","Inclusion Criteria:\n\n1. ≥ 60 years of age at screening\n2. Pelvic pain correlating with fracture location that began EITHER within 6 weeks of a known low-energy traumatic event, OR pelvic insufficiency fracture with pain that is limiting mobility\n3. Diagnostic imaging (X-ray and CT) showing fracture of the pelvis that correlates with pain location\n4. Patient is scheduled for pelvic fixation using at least one iFuse TORQ TNT\n5. Patient and\u002For patient's legally authorized representative (LAR) understands and is willing and able to provide written informed consent\n6. Patient agrees to comply with study schedule of assessments\n7. Patient and\u002For patient's proxy can complete study-related surveys\n8. Patient was able to ambulate prior to index fracture\n\nExclusion Criteria:\n\n1. Any known anatomic issues that could prevent placement of iFuse TORQ TNT\n2. Implants already in the pelvis (e.g. lumbopelvic fixation) that could interfere with placement of the study device(s)\n3. Patient requires lumbosacral pelvic fixation as part of index procedure\n4. Prominent neurologic or uncontrolled psychiatric condition that would interfere with study participation or regaining of physical function related to pelvic fracture and is unable to provide a health care proxy to complete study assessments.\n5. Estimated lifespan \\\u003C 12 months\n6. Presence of tumor, lytic lesion, infection, or soft tissues that precludes safe internal fixation\n7. Not candidate for surgery due to underlying medical illness\n8. Social situation that makes 12-month follow-up unlikely\n9. History of recent (within 1 year) non-index pelvic fracture with non-union\n10. Other clinically active fragility fracture of spine, hip or arms\u002Flegs that could impair recovery from sacral fracture\n11. Known allergy to titanium or titanium alloys\n12. Known or suspected active drug or alcohol abuse, including opioids\n13. Patient is a prisoner or ward of the state\n14. Patient is already participating in an investigational clinical trial that may interfere with implant placement or study follow-up","ALL","60 Years",{"count":19,"type":20},120,"ESTIMATED","OBSERVATIONAL","The purpose of this study is to evaluate outcomes in patients treated with iFuse TORQ TNT for pelvic fragility fractures.",[24,25,26,27,28,29],"Fracture; Pelvic","Insufficiency Fractures","Fragility Fracture","Sacroiliac; Fusion","Sacroiliac Joint Disruption","Sacroiliac Joint Dysfunction",[26,31,32,33],"pelvic fracture","Osteoporotic pelvic fracture","Fragility Fracture of the pelvis","NOT_YET_RECRUITING","2026-04-15",{"date":37,"type":38},"2026-04-20","ACTUAL",{"date":40,"type":20},"2026-08",{"date":42,"type":20},"2028-08",{"name":44,"class":45},"SI-BONE, Inc.","INDUSTRY",{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":52,"eligibilityCriteria":53,"healthyVolunteers":11,"sex":16,"minAge":54,"maxAge":4,"enrollmentInfo":55,"targetDuration":4,"studyType":57,"phases":58,"briefSummary":60,"conditions":61,"keywords":4,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":71,"locationsCount":73},"100608648","lumbar--sacroiliac-fusion-study-involving-previously-implanted-devices-100608648","NCT07204288","Lumbar & Sacroiliac Fusion Study Involving Previously Implanted Devices","Lumbar & Sacroiliac Fusion Study: Multi-Center Prospective Radiographic Study on Subjects Previously Implanted With Spinal Simplicity Lumbar and\u002For Sacroiliac Fusion Device(s)","FUSION","Inclusion Criteria:\n\n1. Be 18 years of age or older at the time of enrollment\n2. Be willing and able to provide informed consent and comply with study visit requirements\n3. Subjects who received a Spinal Simplicity fusion implant(s) (Minuteman G5, Liberty, and\u002For Patriot) between April 1, 2022 and March 31, 2025\n\nExclusion Criteria:\n\n1. Unable to provide consent and complete prospective data collection\n2. Women who are pregnant, or may become pregnant, during the course of the study\n3. Contraindication to CT scanning, in the opinion of the investigator","18 Years",{"count":56,"type":20},500,"INTERVENTIONAL",[59],"NA","This study is a multi-center, observational, prospective and retrospective data collection study",[62,27],"Fusion of Spine","RECRUITING","2026-03-16",{"date":66,"type":38},"2026-03-18",{"date":68,"type":38},"2025-09-11",{"date":70,"type":20},"2026-12",{"name":72,"class":45},"Spinal Simplicity LLC",3,{"id":75,"slug":76,"hasResults":11,"nctId":77,"briefTitle":78,"officialTitle":78,"acronym":4,"eligibilityCriteria":79,"healthyVolunteers":11,"sex":16,"minAge":54,"maxAge":4,"enrollmentInfo":80,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":82,"conditions":83,"keywords":87,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":93,"lastUpdatePostDateStruct":94,"startDateStruct":96,"completionDateStruct":98,"leadSponsor":100,"locationsCount":103},"100460469","evaluation-of-the-ifuse-bedrock-technique-in-association-with-posterior-lumbosacral-fusion-with-iliac-fixation-100460469","NCT05276024","Evaluation of the IFuse Bedrock Technique in Association with Posterior Lumbosacral Fusion with Iliac Fixation.","Inclusion Criteria:\n\n* Subject scheduled for open posterior lumbosacral arthrodesis (including at least the following three vertebrae: L4, L5 and S1) associated with a sacroiliac fusion procedure and iliac fixation (thoracolumbar fusion procedures extended to sacrum are eligible in the study);\n* Insertion of at least 1 iFuse-3D implant according to the iFuse Bedrock technique (uni- and bilateral insertion are eligible);\n* Subject who preoperatively responded positively to pain provocation tests for SIJ dysfunction with or without a positive SIJ infiltration test;\n* Patient with a degenerative sacroiliac joint disease requested a fusion procedure;\n\nExclusion Criteria:\n\n* Major osteoporosis (DEXA scan \\> 3);\n* Any previous history of sacroiliac joint fusion or any surgical procedure involving a S2-iliac fusion;\n* Subjects requested a SIJ fusion without the iFuse-3D device or iFuse-3D not inserted according to the manufacturer instruction (Bedrock technique);\n* Subjects with a medical or surgical contraindication preventing the intervention from being performed or potentially interfering in the interpretation of the data collected (neurologic condition, local or systemic infection, any known allergy to surgical implants, psychiatric diseases, ...);\n* Currently pregnant or planning pregnancy;\n* Prisoner or a ward of the state;\n* Subject no willing to participate in the study;\n* Subject not affiliated to a social security insurance.",{"count":81,"type":20},50,"The purpose of this study is to describe the impact of the iFuse Bedrock technique to decrease post-operative pains in patients who underwent multilevel posterior lumbosacral fusion.",[84,27,85,86],"Sacroiliitis","Lumbosacral; Fusion","Spine Deformity",[88,89,90,91,92],"Sacroiliac joint pain","Sacroiliac joint fusion","Bedrock technique","Open posterior lumbosacral fusion","Spine deformties","2024-11-06",{"date":95,"type":38},"2024-11-08",{"date":97,"type":38},"2022-06-10",{"date":99,"type":20},"2026-04-01",{"name":101,"class":102},"Polyclinique Bordeaux Nord Aquitaine","OTHER",2,{"id":105,"slug":106,"hasResults":11,"nctId":107,"briefTitle":108,"officialTitle":109,"acronym":110,"eligibilityCriteria":111,"healthyVolunteers":11,"sex":16,"minAge":54,"maxAge":4,"enrollmentInfo":112,"targetDuration":113,"studyType":21,"phases":4,"briefSummary":114,"conditions":115,"keywords":4,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":116,"lastUpdatePostDateStruct":117,"startDateStruct":119,"completionDateStruct":121,"leadSponsor":123,"locationsCount":125},"100553580","real-world-registry-study-on-patient-satisfaction-with-transloc-3d-si-joint-fusion-100553580","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",{"count":19,"type":20},"18 Months","This is a multi-center, consecutive enrollment registry study to evaluate patient satisfaction post SI Fusion with the TransLoc 3D SI Fusion System.",[29,27],"2024-08-21",{"date":118,"type":38},"2024-08-23",{"date":120,"type":38},"2024-08-15",{"date":122,"type":20},"2024-12-15",{"name":124,"class":45},"CornerLoc",1]