[{"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":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,55,79],{"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":36,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":43,"lastUpdatePostDateStruct":44,"startDateStruct":47,"completionDateStruct":49,"leadSponsor":51,"locationsCount":54},"100651571","phase-4-success-rates-and-safety-of-steroid-injections-in-managing-spinal-and-sacro-iliac-pain-cortisone-injection-spine-study-100651571",false,"NCT07762170","Success Rates and Safety of Steroid Injections in Managing Spinal and Sacro-Iliac Pain (CORTisone Injection Spine Study)","Success Rates and Safety in Managing Spinal and Sacro-Iliac Pain: A Critical Analysis","CORTISS","Inclusion Criteria:\n\n* \\>18 years of age;\n* Diagnosis of lumbar, cervical, or thoracic pain with various etiologies;\n* Eligibility to receive steroid injections for back pain, including epidural, facet joints, or SIJ injections, or other injections (e.g., local anesthetics);\n* Being willing and able to provide NRS pain ratings and PROMIS functionality ratings before the intervention, and the same scores plus IPR, fIPR, and PGIC at various follow-up points after the intervention;\n* Provide written informed consent.\n\nExclusion Criteria:\n\n* Diagnosis of dementia, Parkinson's disease or other cognitive impairments;\n* Congenital or acquired polyneuropathy;\n* Back surgery in the month before injection treatment or planned surgery in the subsequent 3 months;\n* Any clinically significant acute or chronic medical condition that in the judgment of Investigator may preclude injection in the epidural space or compromise patient safety, limit patient's ability to complete the study, and\u002For compromise the objectives of the study;\n* Participation in any other competing clinical study within 3 months prior to screening and during the study period.","ALL","18 Years",{"count":20,"type":21},500,"ESTIMATED","INTERVENTIONAL",[24],"PHASE4","This study aims to analyze the efficacy and safety of different kinds of steroid injections for back pain, comparing different steroids, dosages, locations (epidural, facet joints, nerve blocks), and also the difference between injections with steroids and local anesthetics, to optimize this treatment that is currently not standardized. The investigators will compare retrospectively and prospectively the efficacy of different injections in the same patients, using mainly a parameter called integral of pain relief, which combines the percentage of pain relief provided by a treatment and its duration over time, as well as improvements in functionality.",[27,28,29,30,31,32,33,34,35],"Back Pain Lower Back","Neck Pain","Radiculopathy Multiple Sites","Spinal Stenosis Cervicothoracic Region","Spinal Stenosis Lumbar","Failed Back Surgery Syndrome (FBSS)","Sciatica","Intervertebral Disc Disorders With Radiculopathy, Lumbar Region","Spine Osteoarthritis",[37,38,39,40,41],"epidural steroid injections","back pain treatments","pain relief","spinal steroid injections","spinal injections","RECRUITING","2026-08-07",{"date":45,"type":46},"2026-08-13","ACTUAL",{"date":48,"type":46},"2026-07-30",{"date":50,"type":21},"2030-03",{"name":52,"class":53},"Igor Wilderman. MD","OTHER",1,{"id":56,"slug":57,"hasResults":11,"nctId":58,"briefTitle":59,"officialTitle":59,"acronym":60,"eligibilityCriteria":61,"healthyVolunteers":11,"sex":17,"minAge":62,"maxAge":4,"enrollmentInfo":63,"targetDuration":4,"studyType":65,"phases":4,"briefSummary":66,"conditions":67,"keywords":4,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":54},"100623107","a-prospective-cohort-study-of-basivertebral-nerve-ablation-using-the-stryker-optablate-bvn-system-for-the-treatment-of-vertebrogenic-low-back-pain-100623107","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","22 Years",{"count":64,"type":21},25,"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.",[68,27],"Verteborgenic Low Back Pain","2026-06-16",{"date":71,"type":46},"2026-06-18",{"date":73,"type":46},"2026-06-02",{"date":75,"type":21},"2027-11-30",{"name":77,"class":78},"Stryker Instruments","INDUSTRY",{"id":80,"slug":81,"hasResults":11,"nctId":82,"briefTitle":83,"officialTitle":84,"acronym":4,"eligibilityCriteria":85,"healthyVolunteers":11,"sex":17,"minAge":86,"maxAge":87,"enrollmentInfo":88,"targetDuration":4,"studyType":22,"phases":90,"briefSummary":92,"conditions":93,"keywords":4,"overallStatus":95,"whyStopped":4,"lastUpdateSubmitDate":96,"lastUpdatePostDateStruct":97,"startDateStruct":99,"completionDateStruct":101,"leadSponsor":103,"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":89,"type":21},60,[91],"NA","Determine whether high intensity focused electromagnetic therapy has a significant effect on pain and quality of life in patients with lumbar disc prolapse.",[27,94],"Magnetic Therapy","NOT_YET_RECRUITING","2025-12-01",{"date":98,"type":46},"2025-12-12",{"date":100,"type":21},"2025-12-07",{"date":102,"type":21},"2026-04-01",{"name":104,"class":53},"Middle East University"]