[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"spinal-fracture\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:spinal-fracture":94},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,49,77],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":31,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100640245","evaluation-of-the-evolution-of-patient-care-within-the-spinal-pathology-department-100640245",false,"NCT07627282","Evaluation of the Evolution of Patient Care Within the Spinal Pathology Department","Evaluation of the Evolution of the Quality of Life of Patients Treated by the Spinal Pathology Department","SPINDATA","Inclusion criteria:\n\n* Patient \\> 18 years old\n* Minor patient, able to accept the data collection, with the consent of the holder(s)\n* Patient consulting for a medical reason involving a spinal pathology in the investigating center (spinal surgery department): Degenerative pathology of the thoracic or lumbar spine; Degenerative pathology of the cervical spine; Deformation of the spine; Urgent traumatic, infectious and tumor pathologies.\n\nExclusion criteria:\n\n* Patient under guardianship or curators,\n* Persons deprived of liberty by judicial or administrative decision,\n* Persons undergoing psychiatric treatment under duress requiring the consent of the legal representative\n* Persons unable to express their consent,\n* Persons under legal protection,\n* Patient not affiliated to a social protection scheme.","ALL","18 Years",{"count":20,"type":21},15000,"ESTIMATED","INTERVENTIONAL",[24],"NA","Spinal conditions are a major public health issue. Their management by surgical treatment is constantly improving and surgical procedures or implantable medical devices are experiencing significant progress. These innovations have not yet all been precisely evaluated but have already led to significant changes in care practices. The primary objective of our study is to describe, via an exhaustive collection of data, the quarterly evolution over 5 years of practices in the management of spinal pathologies.",[27,28,29,30],"Spinal Stenosis","SPINAL Fracture","Vertebral Osteomyelitis","Vertebral Metastasis",[32,33,34,35],"spine","care","surgery","evolution","RECRUITING","2026-05-29",{"date":39,"type":40},"2026-06-04","ACTUAL",{"date":42,"type":40},"2023-05-25",{"date":44,"type":21},"2031-08",{"name":46,"class":47},"University Hospital, Bordeaux","OTHER",1,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":55,"eligibilityCriteria":56,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":57,"enrollmentInfo":58,"targetDuration":4,"studyType":22,"phases":60,"briefSummary":61,"conditions":62,"keywords":65,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":76},"100498350","surgical-versus-non-surgical-treatment-of-thoracolumbar-burst-fracture-100498350","NCT05769114","Surgical Versus Non-Surgical Treatment of Thoracolumbar Burst Fracture","Outcome of Surgical Versus Primary Non-Surgical Treatment of Traumatic Thoracolumbar Spine Burst Fracture in Patients Without Neurological Symptoms: A Randomized Controlled Clinical Trial","A34RCT","Inclusion Criteria:\n\n* Age 18 - 70 years at inclusion\n* Acute traumatic burst fracture of the thoracolumbar spine (10th thoracic to 3rd lumbar vertebral body)\n* Informed consent for study participation\n\nExclusion Criteria:\n\n* Injury of the posterior tension band\u002Fposterior column of the thoracolumbar spine\n* Any neurological deficit (American Spinal Injury Association Impairment Scale \\[AISA\\] Grade A-D)\n* Pathological vertebral body fractures (diagnosed by MRI and CT scan), which, in the opinion of the research\u002Finvestigative team, would compromise (or interfere with) patients' ability to participate in the study\n* Concomitant spinal fractures at any other level of the spine outside the T10-L3 level, which, in the opinion of the research\u002Finvestigative team, would compromise (or interfere with) patients' ability to participate in the study\n* Multiple trauma or Injury Severity Score (ISS) \\> 16 or additional injuries according to the investigator may, which, in the opinion of the research\u002Finvestigative team, would compromise (or interfere with) patients' ability to participate in the study (impairment of early ambulation)\n* Any known previous spinal surgery in the thoracolumbar spine, which, in the opinion of the research\u002Finvestigative team, would compromise (or interfere with) patients' ability to participate in the study\n* Any severe, progressive, or uncontrolled medical or psychiatric condition, or other factors at randomization that in the judgment of the investigator prevents the patient from participating in the study\n* Known history of substance abuse (i.e., recreational drugs, alcohol) that would preclude reliable assessment in the opinion of the investigator\n* Pregnancy or women planning to conceive within the study period. All women included in this study must have a negative blood pregnancy test (human chorionic gonadotrophin (hCG) blood level at visit 1. If pregnancy occurs during the study period, the patients drop out of the study\n* Inability to follow the procedures of the study, e.g., due to inability to understand German, French or English, which, according to the investigator, may jeopardize the patient in case of participation in the study or prevents the patient from participating in the study","70 Years",{"count":59,"type":21},52,[24],"Treatment for acute traumatic thoracolumbar burst fractures differs significantly across the world in patients without neurological impairments and without damage to the posterior column of the spine. This randomized controlled, non-inferiority clinical trial's goal is to evaluate the effectiveness of surgery versus initial non-surgical treatment for patients with traumatic thoracolumbar spine burst fractures who don't have any neurological symptoms.\n\nThe study's precise objectives are to:\n\n1. evaluate the clinical outcome (Oswestry Disability Index)\n2. evaluate the radiography result (restoration and maintenance of spinal alignment)\n3. determine the prevalence of complications\n\nat least 24 months of follow-up of neurologically unaffected patients with acute traumatic burst fractures. Both groups will get the same therapy using standardized methods: The surgical group's entire patient population will get combined anterior-posterior (360°) spinal fusion therapy. Three-point hyperextension orthoses will be used to treat all patients in the non-surgical group for six weeks following the injury.",[28,63,64],"Burst Fracture","Spinal Instability of Thoracolumbar Region",[66],"Traumatic Thoracolumbar Spine Burst Fracture","2026-05-01",{"date":69,"type":40},"2026-05-07",{"date":71,"type":40},"2023-04-18",{"date":73,"type":21},"2030-03",{"name":75,"class":47},"Insel Gruppe AG, University Hospital Bern",2,{"id":78,"slug":79,"hasResults":11,"nctId":80,"briefTitle":81,"officialTitle":82,"acronym":83,"eligibilityCriteria":84,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":85,"targetDuration":4,"studyType":87,"phases":4,"briefSummary":88,"conditions":89,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":95,"lastUpdatePostDateStruct":96,"startDateStruct":98,"completionDateStruct":100,"leadSponsor":102,"locationsCount":48},"100452385","clariance-erys-registry-100452385","NCT05170815","Clariance ErYs Registry","Clariance Registry of ERISMA® and Idys® Devices","ErYs","Inclusion Criteria:\n\n* Considered as adult in the respective geography (18 years old or older for France and 21 years old or older for United-States).\n* Indicated for treatment with one or more commercially available sponsor spine device included into the study.\n* For France only, affiliated with or beneficiary of a social security scheme.\n\nExclusion Criteria:\n\n* Subjects who are not able to comply with the study procedures based on the judgment of the investigator (e.g., inability to comprehend study related questions, inability to keep scheduled assessment times).\n* Subjects who are considered as vulnerable: minor, pregnant woman or people under legal protection (guardianship or curatorship).\n* Contraindicated for spine surgery utilizing a commercially available sponsor spine device.",{"count":86,"type":21},760,"OBSERVATIONAL","International, prospective, single arm, multicenter and observational Post-Market Clinical Follow-up (PMCF).\n\nThe overall objective of this study is to collect preoperative, intraoperative and postoperative (at 9 weeks, 6 months, 1 year and 2 years) data on the clinical complications and functional outcomes of the study devices to demonstrate safety and performance in a real-world setting.\n\nThe primary objective is to demonstrate that the use of the study devices is safe.\n\nThe secondary objective is to demonstrate that the use of the study devices decreases the pain, and improves the quality of life and the daily activities of the subjects.",[90,91,92,93,94],"Spine Degeneration","Spine Spondylosis Thoracic","Spinal Deformity","Spinal Tumor","Spinal Fracture","2026-03-16",{"date":97,"type":40},"2026-03-17",{"date":99,"type":40},"2022-01-17",{"date":101,"type":21},"2028-12",{"name":103,"class":104},"Clariance","INDUSTRY"]