[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"complex-regional-pain-syndrome-crps\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:complex-regional-pain-syndrome-crps":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,48,77],{"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":28,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100620751","effectiveness-of-transcranial-direct-current-stimulation-tdcs-in-the-management-of-complex-regional-pain-syndrome-100620751",false,"NCT07361692","Effectiveness of Transcranial Direct Current Stimulation (tDCS) in the Management of Complex Regional Pain Syndrome","Study of the Effectiveness of Transcranial Direct Current Stimulation (tDCS) in the Management of Complex Regional Pain Syndrome","ALGOSTIM","Inclusion Criteria:\n\n* Major\n* Clinically active or active complex regional pain syndrome (CRPS) with positive Budapest criteria\n* Scintigraphy showing signs consistent with CRPS\n* Being affiliated with or a beneficiary of a social security scheme\n\nExclusion Criteria:\n\n* Algodystrophy no longer meeting the Budapest criteria\n* Relative contraindication to tDCS: psychosis (including treated psychosis), uncontrolled epilepsy, large scalp scar, intracerebral\u002Fintracranial metallic body\n* Pregnant or breastfeeding women\n* Minors\n* Persons under legal protection (guardianship, conservatorship, and protective supervision)\n* Persons deprived of their liberty by judicial or administrative order\n* Unwilling individuals who cannot give their consent or cannot return for scheduled visits according to the protocol","ALL","18 Years",{"count":20,"type":21},32,"ESTIMATED","INTERVENTIONAL",[24],"NA","Transcranial direct current stimulation (tDCS) is a non-invasive therapy increasingly used in facilities treating patients with chronic pain. This complementary therapy has the advantage of being non-pharmacological, with transient and mild side effects, an excellent safety profile, and good efficacy in the contexts where it has been the subject of dedicated research: neuropathic pain, fibromyalgia, and visceral pain. Few studies have focused on the application of tDCS in the context of complex regional pain syndrome (CRPS), which is a common condition.",[27],"Complex Regional Pain Syndrome (CRPS)",[29,30,31,32,33,34],"Transcranial direct current stimulation","Complex Regional Pain Syndrome","pain","quality of life","anxiety","central sensitization","RECRUITING","2026-06-17",{"date":38,"type":39},"2026-06-18","ACTUAL",{"date":41,"type":39},"2026-04-01",{"date":43,"type":21},"2027-06",{"name":45,"class":46},"Polyclinique de l'Europe","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":55,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":56,"targetDuration":4,"studyType":58,"phases":4,"briefSummary":59,"conditions":60,"keywords":63,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":47},"100619788","peripersonal-space-representation-in-upper-limb-segmental-exclusion-100619788","NCT07349173","Peripersonal Space Representation in Upper Limb Segmental Exclusion","Study of the Representation of Action Peripersonal Space in Participants With Unilateral Segmental Exclusion of the Upper Limb Compared to Asymptomatic Subjects","Inclusion Criteria (patients):\n\n* Age ≥ 18 years.\n* Presenting unilateral exclusion symptom of the upper limb or part of the hand evolving for \\> 3 months.\n* No contraindication to force work in daily activities.\n* For patients with finger exclusion: at least 2 perturbed items related to exclusion on tests 3 and 4 of the \"Bilan 400 points\".\n* Affiliated to a social security scheme.\n* Able to understand simple orders.\n\nInclusion Criteria (Controls):\n\n* Age ≥ 18 years.\n* No history of upper limb impairment with sequelae.\n\nExclusion Criteria (All):\n\n* Visual impairments.\n* Central neurological pathology.\n* Unstabilized psychiatric pathology.\n* Communication or comprehension difficulties.\n* Under legal protection or unable to consent.\n* Pregnant or breastfeeding women.\n* Cervical pathology contraindicating VR headset use.\n* Epilepsy.\n* Upper limb pathology unrelated to exclusion.\n* Inability to stand for 40 minutes.",true,{"count":57,"type":21},60,"OBSERVATIONAL","This study aims to evaluate the representation of action peripersonal space (PPS) in subjects suffering from unilateral segmental exclusion syndrome of the upper limb compared to healthy control subjects. Segmental exclusion is defined by non-use or under-use of a limb segment without central nervous system damage. The study hypothesizes that this syndrome leads to a modification (shrinkage) of the PPS representation. Participants will perform reachability judgments in a Virtual Reality (VR) environment.",[61,27,62],"Segmental Exclusion Syndrome","Upper Limb Neglect (Peripheral)",[64,65,66,67],"Peripersonal Space","Virtual Reality","Body Schema","Reachability Judgment","2026-03-12",{"date":70,"type":39},"2026-03-16",{"date":72,"type":39},"2025-12-04",{"date":74,"type":21},"2028-01",{"name":76,"class":46},"Union de Gestion des Etablissements des Caisses d'Assurance Maladie - Nord Est",{"id":78,"slug":79,"hasResults":11,"nctId":80,"briefTitle":81,"officialTitle":82,"acronym":4,"eligibilityCriteria":83,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":84,"enrollmentInfo":85,"targetDuration":4,"studyType":22,"phases":87,"briefSummary":88,"conditions":89,"keywords":90,"overallStatus":96,"whyStopped":4,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":47},"100592001","reducing-pain-in-complex-regional-pain-syndrome-using-personalized-brain-stimulation-a-feasibility-study-100592001","NCT06987747","Reducing Pain in Complex Regional Pain Syndrome Using Personalized Brain Stimulation: A Feasibility Study","Reducing Pain in CRPS Using Personalized Brain Stimulation: A Feasibility Study","Inclusion Criteria:\n\n* Diagnosis of CRPS Type 1 affecting the upper or lower limb using the revised Budapest criteria\n* History of CRPS of at least 3 months since the start of symptoms or diagnosis\n\nExclusion Criteria:\n\n* CRPS diagnosis greater than 3 years to avoid patients with chronic CRPS who may not respond to interventions\n* Contraindications to transcranial magnetic stimulation (TMS)\n* Known psychological diagnosis affecting comprehension\n* Prior experience with TMS\n* Inability to participate in the study","70 Years",{"count":86,"type":21},10,[24],"This research study looks at the feasibility of using a new treatment, noninvasively activating the brain through repetitive transcranial magnetic stimulation (rTMS) to treat pain symptoms of complex regional pain syndrome (CRPS). This study will help us determine if this technique is feasible (able to recruit participants and if the research activities are feasible and can be used to treat CRPS patients with pain in a larger study. The investigators will also examine how TMS can be personalized to individuals using an individual's brain activity measured using EEG. The investigators will also study whether the effects of TMS are stronger if the TMS is delivered during a specific timing of the EEG activity.",[27],[91,92,30,93,94,95],"repetitive transcranial magnetic stimulation","personalized repetitive transcranial magnetic stimulation","CRPS","Electroencephalogram","EEG guided TMS","NOT_YET_RECRUITING","2025-05-22",{"date":99,"type":39},"2025-05-23",{"date":101,"type":21},"2025-07-01",{"date":103,"type":21},"2026-02-01",{"name":105,"class":46},"McMaster University"]