[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100505157":3},{"organization":4,"armGroups":7,"interventions":13,"overallOfficials":18,"centralContacts":19,"locations":25,"responsibleParty":43,"collaborators":18,"id":45,"slug":46,"hasResults":47,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":51,"eligibilityCriteria":52,"healthyVolunteers":47,"sex":53,"minAge":54,"maxAge":55,"enrollmentInfo":56,"targetDuration":18,"studyType":59,"phases":60,"briefSummary":62,"conditions":63,"keywords":65,"overallStatus":28,"whyStopped":18,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":77},{"fullName":5,"class":6},"Centre Hospitalier Universitaire de Nice","OTHER",[8],{"label":9,"type":6,"description":10,"interventionNames":11},"neurostimulation","3 months of tonic stimutaltion + 3 weeks with random stimulation mode between microburst, High frequency, stopped stimulation (Off) then stimulation with the more efficient mode (according the patient) until 6 monthe after implantation.",[12],"Other: walking quantified analysis",[14],{"type":6,"name":15,"description":16,"armGroupLabels":17,"otherNames":18},"walking quantified analysis","Test to measure anthropometry, joint amplitudes, muscle strength and spasticity of the lower limbs on a treadmill.",[9],null,[20],{"name":21,"role":22,"phone":23,"phoneExt":18,"email":24},"LE GOFF Ludovic, MD","CONTACT","+334 92 03 55 07","legoff.l@chu-nice.fr",[26],{"facility":27,"status":28,"city":29,"state":18,"zip":30,"country":31,"countryCode":32,"cosmosGeoPoint":33,"geoPoint":38,"contacts":39},"Chu de Nice","RECRUITING","Nice","06200","France","FR",{"type":34,"coordinates":35},"Point",[36,37],7.26608,43.70313,{"lat":37,"lon":36},[40],{"name":41,"role":22,"phone":42,"phoneExt":18,"email":24},"LE GOFF Ludovic","+33492035507",{"type":44,"investigatorFullName":18,"investigatorTitle":18,"investigatorAffiliation":18,"oldNameTitle":18,"oldOrganization":18},"SPONSOR","100505157","improvement-of-gait-by-spinal-stimulation-in-patients-with-postoperative-chronic-lumbosciatalgia-pilot-study-gaitstim-100505157",false,"NCT05857696","Improvement of Gait by Spinal Stimulation in Patients With Postoperative Chronic Lumbosciatalgia: Pilot Study (GaitStim)","Study of the Improvement of Gait by Spinal Stimulation in Patients With Post-operative Chronic Lumbosciatalgia: Pilot Study","GAITSTIM","Inclusion Criteria:\n\n* Age \\> 18 year old and \\\u003C or = 70 year old\n* Patients with chronic neuropathic lumbo-sciatalgia (DN4 score \\> or = 4\u002F10) as part of a moderate to severe spinal surgery failure syndrome (EVA \\>50\u002F100), in who a collegial and multidisciplinary indication of medullary stimulation treatment was chosen.\n* Patients awith Social Security\n\nExclusion Criteria:\n\n* Vulnerable persons\n* Patients who are invalid and unable to perform a quantified walk analysis\n* Contraindication to surgery or anesthesia\n* Patient not able to complete questionnaires\n* Woman of childbearing age without effective contraception","ALL","18 Years","70 Years",{"count":57,"type":58},36,"ESTIMATED","INTERVENTIONAL",[61],"NA","The purpose of this study is to explore the changes in objective walking parameters induced by medullary stimulation in patients with Fail Back Surgery Syndrome, after chronic stimulation, in comparison with preoperative condition.",[64],"Failed Back Surgery Syndrome",[66,67],"Spinal cord neurostimulation","chronic pain","2026-06-15",{"date":70,"type":71},"2026-06-16","ACTUAL",{"date":73,"type":71},"2024-02-23",{"date":75,"type":58},"2028-10-23",{"name":5,"class":6},1]