[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"lumbar-pain-syndrome\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:lumbar-pain-syndrome":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,48,79,117],{"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":4,"briefSummary":23,"conditions":24,"keywords":31,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100635425","patient-reported-outcome-measurements-registration-in-spinal-pathologies-and-neuromodulation-100635425",false,"NCT07552519","Patient Reported Outcome Measurements Registration in Spinal Pathologies and Neuromodulation","Patient Reported Outcome Measurements Registration in Spinal Pathologies and Neuromodulation: a Prospective Real-world Data Collection With Pre-determined Follow-up Moments","PROMSPINE","Inclusion Criteria:\n\n1. Clinical diagnosis of spinal disease\n2. Clinical indication to perform treatment of this disease\n3. willing and capable to provide informed consent\n4. Age ≥18 y\n\nExclusion Criteria:\n\nnot able to provide consent","ALL","18 Years",{"count":20,"type":21},5000,"ESTIMATED","OBSERVATIONAL","Longitudinal prospective observational data collection with questionnaires and categorical diagnostic and therapeutic registration and follow-up in spinal pathologies and neuromodulation",[25,26,27,28,29,30],"Spinal Pathologies","Pain","Cervical Pain","Lumbar Pain Syndrome","Neurostimulation","Disc Degenerative Disease",[32,33,34],"neuromodulation","pain","spinal pathologies","RECRUITING","2026-04-20",{"date":38,"type":39},"2026-04-27","ACTUAL",{"date":41,"type":21},"2026-04",{"date":43,"type":21},"2030-06-01",{"name":45,"class":46},"Jessa Hospital","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":54,"eligibilityCriteria":55,"healthyVolunteers":11,"sex":17,"minAge":56,"maxAge":57,"enrollmentInfo":58,"targetDuration":4,"studyType":60,"phases":61,"briefSummary":63,"conditions":64,"keywords":65,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":71,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":47},"100597662","impact-of-a-multidisciplinary-rehabilitation-program-associated-with-the-doado-application-in-lowback-pain-management-100597662","NCT07061405","Impact of a Multidisciplinary Rehabilitation Program Associated With the Doado Application in Lowback Pain Management","Impact of a Multidisciplinary Rehabilitation Program and Doado Application on the Functional Disability of Patients With Low Back Pain at Risk of Chronicization, Compared With a Monodisciplinary Rehabilitation Program and Doado Application.","REEDUCALGIE","Inclusion Criteria:\n\nPatient:\n\n1. Suffering from acute common low back pain for less than 3 months at the time of the initial consultation\n2. With a prescription for physiotherapy\n3. Available for both programs\n4. Aged between 20 and 55\n5. Equipped with a smartphone compatible with the Doado application\n6. Having been informed and having signed the free and informed consent form prior to any specific study procedure\n7. Affiliated to a health insurance scheme\n\nExclusion Criteria:\n\nPatient:\n\n1. suffering from a first episode of acute common low back pain for less than one month at the time of the initial consultation\n2. With a history of spinal surgery:\n\n   1. For lumbar arthrodesis in the 12 months prior to inclusion\n   2. For lumbar arthroplasty in the 6 months prior to inclusion\n   3. For lumbar recalibration or lumbar disc herniation within 3 months of inclusion.\n3. With suspected specific low-back pain\n4. Suffering from radiculalgia of the lower limbs\n5. Suffering from sensory-motor disorders of the lower limbs\n6. Suffering from continuous low-back pain for at least 3 months\n7. Have severely impaired physical and\u002For psychological health, which in the investigator's opinion may affect the participant's compliance with the study.\n8. Participating in other interventional research\n9. In a period of exclusion from other research still in progress at the time of inclusion.\n10. Protected: adult under guardianship, curatorship or other legal protection, deprived of liberty by judicial or administrative decision.\n11. Pregnant, breast-feeding or parturient.","20 Years","55 Years",{"count":59,"type":21},84,"INTERVENTIONAL",[62],"NA","This study is aimed at patients consulting a physiotherapist for acute low-back pain at risk of becoming chronic.\n\nThe goal of this study is to compare two types of rehabilitation programs for these patients, on their functional disability at 3 months:\n\n* A multidisciplinary program lasting two weeks, including physiotherapists, rheumatologists, physical medicine and rehabilitation specialists, occupational physicians, psychologists, etc.\n* A monodisciplinary physiotherapy rehabilitation program consisting of active treatment with a physiotherapist, with 2 to 3 sessions per week for 4 to 5 weeks, based on muscle-strengthening exercises for the trunk and lower limbs and stretching exercises for the back and lower limbs.\n\nPatients will be evaluated before treatment (baseline), and at 1, 3, 6 and 12 months to evaluate the following secondary outcomes: pain, absence of chronicity, evolution of functional disability, muscle endurance, flexibility, level of fear, apprehension and avoidance associated with low back pain over the time, return to work and to physical activities, painful relapses and analgesic treatment consumption.",[28],[66,67,68,69],"rehabilitation","functional disability","multidisciplinary program","physiotherapy","NOT_YET_RECRUITING",{"date":72,"type":39},"2026-04-23",{"date":74,"type":21},"2026-05",{"date":76,"type":21},"2028-11",{"name":78,"class":46},"Elsan",{"id":80,"slug":81,"hasResults":11,"nctId":82,"briefTitle":83,"officialTitle":84,"acronym":85,"eligibilityCriteria":86,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":87,"targetDuration":4,"studyType":60,"phases":89,"briefSummary":90,"conditions":91,"keywords":101,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":108,"lastUpdatePostDateStruct":109,"startDateStruct":111,"completionDateStruct":113,"leadSponsor":115,"locationsCount":47},"100579522","auriculotherapy-neuroimaging-100579522","NCT06825390","AuriculoTherapy NeuroImaging","Mechanistic Clinical Trial of Auricular Stimulation and Cryogenic Auriculotherapy in Patients With Chronic Low-back Pain, Using Functional Near-infrared Spectroscopy and Magnetic Resonance Imaging","ATNI","Inclusion Criteria:\n\n1. Adult, at least 18 years old\n2. Episodes of chronic low back pain at least daily for at least 6 months, with an average pain score within the last week of 3\u002F10.\n\nExclusion Criteria:\n\n1. active lesions, skin disruptions, or neuropathy of either ear;\n2. recent (\\\u003C1 month) analgesic procedures or surgery;\n3. recent (\\\u003C1 month) start of new analgesic or psychoactive medication (including marijuana, opioids, tramadol, methadone, gabapentinoids, anti-depressants, anti-epileptics, mood-stabilizers, anti-psychotics, or stimulants);\n4. history of chronic pain in shoulder or thumb (to avoid confounding at control stimulation points);\n5. recent (\\\u003C 3 months) illicit drug use;\n6. prior substance misuse\u002Fabuse;\n7. cold-activated diseases (including: agammaglobulinemia, cold urticaria, cold agglutinin disease, cryofibrinogenemia, cryoglobulinemia, immunosuppression, Raynaud's disease, collagen or autoimmune diseases, multiple myeloma, platelet deficiency disorders, pyoderma gangrenosum.)\n\n   \\- MRI-specific exclusions additionally include:\n8. Pregnancy or active attempts at conception;\n9. Implanted metal or electronic device;\n10. severe claustrophobia",{"count":88,"type":21},60,[62],"This is a clinical study of patients who have low back pain (for at least 6 months). The goal is to understand, with brain imaging, how auriculotherapy (an acupuncture-like stimulation of the ear) may work to relieve pain. There are 4 total study visits, divided into two pairs of visits that occur before and 5-7 days after receiving either a real or sham auriculotherapy treatment. The cryo-IQ device will be used, to stimulate 7 small areas on both ears with a focused jet of cold as a small amount of compressed gas is released. This is generally not painful, and less invasive, compared to using needles for auriculotherapy.",[92,93,94,95,96,28,97,98,99,100],"Low Back Pain","Chronic Low-back Pain","Back Pain, Low","Lumbar Disc Disease","Lumbar Discogenic Pain","Lumbar Post-Laminectomy Syndrome","Back Pain Lower Back Chronic","Back Pain Without Radiation","Pain;Back Low;Chronic",[102,103,104,105,106,107],"auriculotherapy","auricular stimulation","functional near-infrared spectroscopy","functional magnetic resonance imaging","functional connectivity","cryo-auriculotherapy","2026-02-13",{"date":110,"type":39},"2026-02-18",{"date":112,"type":39},"2025-07-30",{"date":114,"type":21},"2029-04-30",{"name":116,"class":46},"Keith M Vogt",{"id":118,"slug":119,"hasResults":11,"nctId":120,"briefTitle":121,"officialTitle":122,"acronym":4,"eligibilityCriteria":123,"healthyVolunteers":124,"sex":17,"minAge":56,"maxAge":125,"enrollmentInfo":126,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":128,"conditions":129,"keywords":131,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":133,"lastUpdatePostDateStruct":134,"startDateStruct":136,"completionDateStruct":138,"leadSponsor":140,"locationsCount":47},"100512007","caudal-analgesia--anticoagulated-patient-100512007","NCT05946850","Caudal Analgesia & Anticoagulated Patient","Caudal Analgesia in Anticoagulated Chronic Pain Patients","Inclusion Criteria:\n\n* adult chronic pain patients who undergo caudal analgesia\n\nExclusion Criteria:\n\n* chronic pain patients who refuse caudal analgesia",true,"99 Years",{"count":127,"type":21},100,"Caudal analgesia is an effective intervention for lumbosacral pain. Some chronic pain patients take anticoagulants for vasculopathy treatment. Anticoagulation limits the use of caudal analgesia because of the risk of epidural bleeding. Caudal analgesia may be safe and effective in anticoagulated chronic pain patients.\n\nQuantitative analysis of prospective clinical data. Evaluation of caudal analgesia efficacy and safety in anticoagulated chronic pain patients. Analysis of outcome, and complications.",[28,130],"Anticoagulants and Bleeding Disorders",[132],"Caudal analgesia","2025-01-23",{"date":135,"type":39},"2025-01-27",{"date":137,"type":39},"2008-01-02",{"date":139,"type":21},"2025-12-31",{"name":141,"class":46},"Salem Anaesthesia Pain Clinic"]