[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100611175":3},{"organization":4,"armGroups":7,"interventions":22,"overallOfficials":11,"centralContacts":11,"locations":28,"responsibleParty":55,"collaborators":11,"id":57,"slug":58,"hasResults":59,"nctId":60,"briefTitle":61,"officialTitle":61,"acronym":62,"eligibilityCriteria":63,"healthyVolunteers":59,"sex":64,"minAge":65,"maxAge":66,"enrollmentInfo":67,"targetDuration":11,"studyType":70,"phases":71,"briefSummary":73,"conditions":74,"keywords":76,"overallStatus":81,"whyStopped":11,"lastUpdateSubmitDate":82,"lastUpdatePostDateStruct":83,"startDateStruct":86,"completionDateStruct":88,"leadSponsor":90,"locationsCount":91},{"fullName":5,"class":6},"University Hospital, Grenoble","OTHER",[8,14,17],{"label":9,"type":10,"description":11,"interventionNames":12},"Trans-spinal stimulation","ACTIVE_COMPARATOR",null,[13],"Device: Non-invasive device-based neuromodulation",{"label":15,"type":10,"description":11,"interventionNames":16},"Dorsal root ganglion stimulation",[13],{"label":18,"type":19,"description":20,"interventionNames":21},"Placebo (non-stimulation (sham) mode)","PLACEBO_COMPARATOR","The device includes a non-stimulation (sham) mode, which can be activated while still placing the electrodes and setting up the device exactly as in the active condition. In this mode, no effective electrical current is delivered, but the procedure appears identical to the real stimulation. This allows the study to maintain double-blind conditions",[13],[23],{"type":24,"name":25,"description":26,"armGroupLabels":27,"otherNames":11},"DEVICE","Non-invasive device-based neuromodulation","Direct current stimulation (tsDCS) protocol consist of one daily session for five consecutive days during the first week, followed by one session per week until week 5, after which the treatment period ends and post-treatment follow-up begins.",[15,18,9],[29,40],{"facility":30,"status":11,"city":31,"state":11,"zip":11,"country":32,"countryCode":33,"cosmosGeoPoint":34,"geoPoint":39,"contacts":11},"Clinical Neurophysiology Unit, Henri Mondor University Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), Créteil, France","Créteil","France","FR",{"type":35,"coordinates":36},"Point",[37,38],2.46569,48.79266,{"lat":38,"lon":37},{"facility":41,"status":11,"city":42,"state":11,"zip":43,"country":32,"countryCode":33,"cosmosGeoPoint":44,"geoPoint":48,"contacts":49},"Pain Management Center, Grenoble Alpes University Hospital (CHU Grenoble Alpes)","Grenoble","38043",{"type":35,"coordinates":45},[46,47],5.71479,45.17869,{"lat":47,"lon":46},[50],{"name":51,"role":52,"phone":53,"phoneExt":11,"email":54},"Pr HODAJ HASAN","CONTACT","+334 76 76 75 75","HHodaj@chu-grenoble.fr",{"type":56,"investigatorFullName":11,"investigatorTitle":11,"investigatorAffiliation":11,"oldNameTitle":11,"oldOrganization":11},"SPONSOR","100611175","evaluation-of-the-analgesic-effect-of-direct-current-stimulation-in-the-treatment-of-pelvic-pain-comparing-three-groups-trans-spinal-stimulation-ganglionic-stimulation-and-placebo-a-randomized-double-blind-study-100611175",false,"NCT07237165","Evaluation of the Analgesic Effect of Direct Current Stimulation in the Treatment of Pelvic Pain, Comparing Three Groups: Trans-spinal Stimulation, Ganglionic Stimulation, and Placebo. A Randomized Double-blind Study","SPINALSTIM","Inclusion Criteria:\n\n* Patient aged 18 to 85 years, suffering from pelvic pain for more than one year (excluding musculoskeletal causes).\n* Patient with stable ongoing medication (analgesic or otherwise) for at least one month.\n* Patient for whom lack of response to conventional treatments has led the pain specialist or referring physician to consider non-pharmacological therapeutic options.\n* Patient reporting a pain intensity score \\>3 on the Numeric Visual Pain Scale (NVPS) during pre-screening.\n* Patient affiliated with the national health insurance system or an equivalent scheme.\n* Patient who has provided written informed consent.\n\nExclusion Criteria:\n\n* History of drug addiction.\n* History of psychiatric disorders likely to interfere with the proper conduct of the study.\n* Patient with skin lesions in the lumbar region.\n* Person unable to understand the study protocol.\n* Individuals covered by Articles L1121-5 to L1121-8 of the French Public Health Code, corresponding to all protected persons: pregnant women, women in labor, breastfeeding mothers, individuals deprived of liberty by judicial or administrative decision, or under legal protection.\n* Subject currently in the exclusion period of another clinical trial","ALL","18 Years","85 Years",{"count":68,"type":69},60,"ESTIMATED","INTERVENTIONAL",[72],"NA","The purpose of this study is to evaluate the analgesic effectiveness of direct current stimulation (tsDCS) in the treatment of pelvic pain by comparing three groups:\n\n* Trans-spinal tsDCS stimulation,\n* Ganglionic tsDCS stimulation,\n* Placebo (sham) tsDCS stimulation.",[75],"Chronic Pelvic Pain",[77,78,79,9,80],"Chronic pelvic pain","Non-invasive spinal cord neuromodulation","Trans-spinal direct current stimulation (tsDCS)","Dorsal root ganglion stimulation (DRGS)","NOT_YET_RECRUITING","2025-11-14",{"date":84,"type":85},"2025-11-19","ACTUAL",{"date":87,"type":69},"2025-12-01",{"date":89,"type":69},"2029-11-01",{"name":5,"class":6},2]