[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"back-pain-lower-back\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:back-pain-lower-back":25},{"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":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":4,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":27,"lastUpdatePostDateStruct":28,"startDateStruct":31,"completionDateStruct":33,"leadSponsor":35,"locationsCount":38},"100623107","a-prospective-cohort-study-of-basivertebral-nerve-ablation-using-the-stryker-optablate-bvn-system-for-the-treatment-of-vertebrogenic-low-back-pain-100623107",false,"NCT07392333","A Prospective Cohort Study of Basivertebral Nerve Ablation Using the Stryker OptaBlate BVN System for the Treatment of Vertebrogenic Low Back Pain","OptaBlate BVN","Inclusion Criteria:\n\n* Patient scheduled for treatment with the OptaBlate BVN System in accordance with the device IFU and willing to participate in the clinical investigation, undergo study procedure, engage in follow-up, able to read, write, speak, and understand English, and able to provide written informed consent.\n\nExclusion Criteria:\n\n* The patient meets one or more contraindications as defined in the locally applicable IFU\n* Spinal fracture or history of spinal trauma at index levels\n* Previous lumbar fusion at any level\n* Prior basivertebral nerve ablation at the target levels\n* Vertebral cancer, spinal metastasis or Tumor-related vertebral fractures\n* History of Osteoporotic vertebral fractures\n* Spine interventions, including epidural steroid injections within 30 days\n* BMI \\> 40 kg\u002Fm²\n* Symptomatic spinal stenosis\n* Radicular pain or leg pain greater than back pain\n* Pregnancy or planning pregnancy during study period\n* Enrollment in another interventional clinical trial\n* Contraindication to MRI\n* Life expectancy of less than 12 months","ALL","22 Years",{"count":19,"type":20},25,"ESTIMATED","OBSERVATIONAL","The goal of this observational study is to evaluate patient outcomes following treatment of vertebrogenic low back pain using the Stryker OptaBlate BVN System. Patients treated in accordance with the device IFU as part of routine clinical care and who consent to participate will be followed for 12 months after the procedure to assess treatment outcomes.",[24,25],"Verteborgenic Low Back Pain","Back Pain Lower Back","RECRUITING","2026-06-16",{"date":29,"type":30},"2026-06-18","ACTUAL",{"date":32,"type":30},"2026-06-02",{"date":34,"type":20},"2027-11-30",{"name":36,"class":37},"Stryker Instruments","INDUSTRY",1,{"id":40,"slug":41,"hasResults":11,"nctId":42,"briefTitle":43,"officialTitle":44,"acronym":4,"eligibilityCriteria":45,"healthyVolunteers":11,"sex":16,"minAge":46,"maxAge":47,"enrollmentInfo":48,"targetDuration":4,"studyType":50,"phases":51,"briefSummary":53,"conditions":54,"keywords":4,"overallStatus":56,"whyStopped":4,"lastUpdateSubmitDate":57,"lastUpdatePostDateStruct":58,"startDateStruct":60,"completionDateStruct":62,"leadSponsor":64,"locationsCount":4},"100614361","high-intensity-focused-electromagnetic-therapy-on-pain-and-quality-of-life-in-patients-with-lumbar-disc-prolapse-100614361","NCT07278596","High Intensity Focused Electromagnetic Therapy on Pain and Quality of Life in Patients With Lumbar Disc Prolapse","Effect of High Intensity Focused Electromagnetic Therapy on Pain and Quality of Life in Patients With Lumbar Disc Prolapse: a Randomized Controlled Trial","Inclusion Criteria:\n\n* A confirmed diagnosis of lumbar disc prolapse by clinical and radiological evaluation.\n* Ages between 30 and 60 years.\n* A history of low back pain for at least three months.\n* A body mass index less than 30 kg\u002Fm².\n\nExclusion Criteria:\n\n* History of spinal surgery or recent traumatic spinal injury.\n* Severe spinal canal stenosis or progressive neurological deficits.\n* Known malignancy, infection, or inflammatory arthritis affecting the spine.\n* Presence of implanted metal devices or pacemakers contraindicating electromagnetic therapy.\n* Pregnancy or suspected pregnancy.\n* Cognitive or psychological disorders that impair communication or ability to follow instructions","30 Years","60 Years",{"count":49,"type":20},60,"INTERVENTIONAL",[52],"NA","Determine whether high intensity focused electromagnetic therapy has a significant effect on pain and quality of life in patients with lumbar disc prolapse.",[25,55],"Magnetic Therapy","NOT_YET_RECRUITING","2025-12-01",{"date":59,"type":30},"2025-12-12",{"date":61,"type":20},"2025-12-07",{"date":63,"type":20},"2026-04-01",{"name":65,"class":66},"Middle East University","OTHER"]