[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Össur Iceland ehf\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":91},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,47,72],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":29,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100606450","evaluating-methods-to-replicate-stumbles-and-slips-during-walking-100606450",false,"NCT07175714","Evaluating Methods to Replicate Stumbles and Slips During Walking","Inclusion Criteria:\n\n* 40 kg \\\u003C body weight \\\u003C 136kg\n* Cognitive ability to understand all instructions and questionnaires in the study\n* Willing and able to participate in the study and following the protocol\n* Age ≥ 18 years\n* Able to walk independently without the use of assistive device such as a cane or walker\n* Able-bodied subjects OR Regular prosthesis users for at least 1 year with unilateral lower limb amputation at or below the transfemoral level (or equivalent level limb deficiency)\n\nExclusion Criteria:\n\n* Subjects with pain which can affect their mobility\n* Users with socket comfort score less than 7\n* Subjects with cognitive impairment\n* Pregnant subjects\n* Musculoskeletal disorders or neurological conditions that affect motor function, gait or balance\n* Use of medications that are known to impair balance and coordination\n* Any other conditions deemed by the investigator to make participation unsafe",true,"ALL","18 Years",{"count":19,"type":20},20,"ESTIMATED","INTERVENTIONAL",[23],"NA","This protocol outlines a study designed to investigate three different methodologies for inducing gait perturbations.\n\nSubjects will be divided into two groups: prosthetic users and able-bodied individuals.\n\nEach group will undergo a series of tests where controlled perturbations are applied using up to three methodologies with the number depending on factors such as time and fatigue. These methodologies may include mechanical, visual, or auditory perturbations designed to mimic unexpected obstacles or changes in terrain.",[26,27,28],"Fall Prevention","Balance, Falls","Amputation of Lower Limb",[30,31,32,33],"amputation","falls","fall prevention","balance","RECRUITING","2026-02-10",{"date":37,"type":38},"2026-02-13","ACTUAL",{"date":40,"type":38},"2025-05-26",{"date":42,"type":20},"2026-12-31",{"name":44,"class":45},"Össur Iceland ehf","INDUSTRY",2,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":4,"eligibilityCriteria":53,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":54,"targetDuration":56,"studyType":57,"phases":4,"briefSummary":58,"conditions":59,"keywords":61,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":63,"lastUpdatePostDateStruct":64,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":71},"100532270","pro-app-prosthetic-outcome-registry-100532270","NCT06210620","Pro APP Prosthetic Outcome Registry","Prospective, Observational Registry to Collect Standard of Care Clinical Testing Data From Lower-limb Prosthesis Patients Via the PRO App.","Inclusion Criteria:\n\nCognitive ability to understand all instructions and questionnaires in the study Willing and able to participate in the study and follow the protocol Individuals with lower limb loss, amputation or deficiency\n\nExclusion Criteria:\n\nNone",{"count":55,"type":20},2000,"10 Years","OBSERVATIONAL","A national, multi-center registry of patients using lower-limb prosthesis, their profiles and devices, and their long-term follow-up and clinical outcomes.",[60],"Amputation",[62],"Registry","2025-09-08",{"date":65,"type":38},"2025-09-15",{"date":67,"type":38},"2024-01-01",{"date":69,"type":20},"2033-09",{"name":44,"class":45},1,{"id":73,"slug":74,"hasResults":11,"nctId":75,"briefTitle":76,"officialTitle":76,"acronym":4,"eligibilityCriteria":77,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":78,"enrollmentInfo":79,"targetDuration":4,"studyType":21,"phases":80,"briefSummary":81,"conditions":82,"keywords":4,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":83,"lastUpdatePostDateStruct":84,"startDateStruct":86,"completionDateStruct":88,"leadSponsor":90,"locationsCount":71},"100434412","clinical-feasibility-of-the-imes-transradial-prosthesis-100434412","NCT04936789","Clinical Feasibility of the IMES Transradial Prosthesis","Inclusion Criteria:\n\n* (unilateral acquired transradial) amputation\n* residual limb size requirements to fit investigational device componentry\n* at least 6 residual muscle locations available for implantation\n* good compliance with health service (rehabilitation)\n* willing to undergo surgical implantation of IMES Sensor implants\n* experience with myoelectric upper limb prostheses\n* using own myoelectric device approximately 6-8h\u002Fday\n* able to provide informed consent and attend the study visits\n\nExclusion Criteria:\n\n* any condition which in the opinion of the investigator poses a risk to health\n* neurological disorder that may prohibit accurate control\n* major injury proximal to the level of amputation\n* neuromuscular disorder\n* nerve transection or palsy that may cause de-innervation of muscles planned for implantation\n* allergy to implanted materials\n* existing active implant","65 Years",{"count":5,"type":20},[23],"This study will evaluate the feasibility of using implanted myoelectric sensors (IMES) to control a transradial prosthesis",[60],"2024-10-04",{"date":85,"type":38},"2024-10-08",{"date":87,"type":38},"2023-01-01",{"date":89,"type":20},"2026-01",{"name":44,"class":45},""]