[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"amputation-of-upper-limb\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:amputation-of-upper-limb":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,45,75],{"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":22,"studyType":23,"phases":4,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100585912","cryo-nerve-block-extremity-amputation-registry-for-post-operative-and-phantom-limb-pain-100585912",false,"NCT06908538","Cryo NerVe Block Extremity AmputatioN RegIStry for Post Operative and pHantom Limb Pain","Cryo NerVe Block Extremity AmputatioN RegIStry for Post Operative and pHantom Limb Pain (VANISH)","VANISH","Inclusion Criteria:\n\n* Patients who have or will have an amputation procedure;\n* Patients who are willing and capable of providing informed consent;\n* Patients whose age is 18 years or above, or of legal age to give informed consent specific to state and national law.\n\nExclusion Criteria:\n\n* Women of childbearing potential who are, or plan to become, pregnant during the time of the study;\n* Other medical, social, or psychological conditions that in the opinion of the Investigator precludes the subject from appropriate consent or adherence to the protocol.","ALL","18 Years",{"count":20,"type":21},2000,"ESTIMATED","5 Years","OBSERVATIONAL","The goal of this Registry is to see how the device is used when freezing nerves during an amputation procedure.",[26,27,28,29,30,31],"Amputation","Amputation of Lower Limb","Amputation of Upper Limb","Amputation, Limb Loss","Amputation, Traumatic\u002FSurgery","Cryo Analgesia","RECRUITING","2026-06-25",{"date":35,"type":36},"2026-06-26","ACTUAL",{"date":38,"type":36},"2025-04-01",{"date":40,"type":21},"2035-04",{"name":42,"class":43},"AtriCure, Inc.","INDUSTRY",5,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":49,"acronym":50,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":52,"targetDuration":4,"studyType":54,"phases":55,"briefSummary":57,"conditions":58,"keywords":60,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":71,"locationsCount":74},"100644134","using-sensorimotor-reorganization-following-upper-limb-amputation-to-improve-prosthetic-control-100644134","NCT07666204","Using Sensorimotor Reorganization Following Upper Limb Amputation to Improve Prosthetic Control","REINVENT","Inclusion Criteria:\n\n* people aged 18 or more\n* amputation or agenesis of one uper limb, above the wrist or higher\n* understanding of the French language and the ability to express onself in that language (for semi-structured interviews)\n* affiliation to a social security programm\n\nExclusion Criteria:\n\n* history of progressive psychiatric or neurological disorders or disorders with residual effects\n* pregnant or breastfeeding woman\n* minor\n* an adult under legal guardianship\n* pain influencing movement (trunk, residual limb, phantom limb, contralateral limb)",{"count":53,"type":21},50,"INTERVENTIONAL",[56],"NA","Amputation of an upper limb results in a disruption of the sensorimotor loop and a reorganization of the nervous system, leading to the emergence of a phantom limb and the adaptation of compensatory motor strategies. This project aims to leverage these phenomena (induced sensations, phantom mobility, and compensations) to improve control, sensory feedback, and the appropriation of prostheses, in order to reduce cognitive load and musculoskeletal disorders.",[28,59],"Agenesis of Upper Limb",[61,62,63],"amputation","amputation of upper limb","prosthesis","2026-06-18",{"date":66,"type":36},"2026-06-24",{"date":68,"type":36},"2026-04-15",{"date":70,"type":21},"2030-04-30",{"name":72,"class":73},"Union de Gestion des Etablissements des Caisses d'Assurance Maladie - Nord Est","OTHER",2,{"id":76,"slug":77,"hasResults":11,"nctId":78,"briefTitle":79,"officialTitle":79,"acronym":80,"eligibilityCriteria":81,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":82,"targetDuration":4,"studyType":54,"phases":84,"briefSummary":85,"conditions":86,"keywords":87,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":90,"lastUpdatePostDateStruct":91,"startDateStruct":93,"completionDateStruct":95,"leadSponsor":97,"locationsCount":99},"100573963","a-multicenter-multinational-cohort-long-term-post-market-clinical-follow-up-pmcf-of-the-safety-and-efficacy-of-the-osseoanchored-prostheses-for-the-rehabilitation-of-amputees-opra-implant-system-when-used-for-transhumeral-implantation-in-amputee-patients-100573963","NCT06753110","A Multicenter, Multinational, Cohort Long-term Post-market Clinical Follow-up (PMCF) of the Safety and Efficacy of the Osseoanchored Prostheses for the Rehabilitation of Amputees (OPRA) Implant System When Used for Transhumeral Implantation in Amputee Patients","ReTHro","Inclusion Criteria:\n\n* Unilateral or bilateral amputation\n* OPRA™ implant system placed, and with S2 completed before 01-Jan-2024\n* Having a minimum of 6 months of follow-up between S2 and enrolment\n\nExclusion Criteria:\n\n* Subject not willing to consent\n* Subject implanted with the e-OPRA system at the humeral level.",{"count":83,"type":21},70,[56],"This non-interventional clinical investigation is initiated for the purpose of long-term Post-Market Clinical Follow-up (PMCF) and the follow-up time of patients is expected to span from 6 months to \\>20 years in function. It will collect and evaluate clinical data on the safety and performance of the OPRA™ Implant System when used on transhumeral amputees and within the scope of the intended use.",[28],[88,89],"Skeletal anchorage of amputation prostheses.","Osseoanchored Prosthesis","2025-06-30",{"date":92,"type":36},"2025-07-03",{"date":94,"type":36},"2025-02-19",{"date":96,"type":21},"2026-03",{"name":98,"class":43},"Integrum",6]