[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Point Designs\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":65},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,44],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":21,"briefSummary":23,"conditions":24,"keywords":26,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100603394","to-evaluate-the-clinical-impact-of-the-point-powered-system-100603394",false,"NCT07135947","To Evaluate the Clinical Impact of the Point Powered System","Inclusion Criteria:\n\n* Partial unilateral hand loss with at least index and\u002For middle fingers amputated at the MCP level\n* Intact thumb with full range of motion\n* Fluent in English\n* Age of 18 years or older\n\nExclusion Criteria:\n\n* Patients with a residual limb that is unhealed from the amputation surgery\n* Unhealed wounds\n* Significant cognitive deficits as determined upon clinical evaluation\n* Significant neurological deficits as determined upon clinical evaluation\n* Significant physical deficits of the residual limb impacting full participation in the study as determined upon clinical evaluation\n* Uncontrolled pain or phantom pain impacting full participation in the study as determined upon clinical evaluation\n* Serious uncontrolled medical problems as judged by the project therapist","ALL","18 Years",{"count":18,"type":19},10,"ESTIMATED","INTERVENTIONAL",[22],"NA","The objective of this study is to evaluate the efficacy of the Point Powered system as compared to the patient's standard-of-care treatment. This study will be a single subject crossover design where one group of 10 adult partial hand amputees will be evaluated on several metrics on their existing prosthetic treatment (Treatment 1) and the Point Powered system (Treatment 2) over a period of three months using standard two-site myoelectric control. Metrics include: in-clinic functional measures, subjective assessments, bilateral hand use, and prosthesis wear time.",[25],"Amputation; Traumatic, Hand",[27,28,29,30],"Prosthesis","Myoelectric","Digits","Fingers","NOT_YET_RECRUITING","2026-06-23",{"date":34,"type":35},"2026-06-26","ACTUAL",{"date":37,"type":19},"2026-09-01",{"date":39,"type":19},"2027-04-01",{"name":41,"class":42},"Point Designs","INDUSTRY",3,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":48,"acronym":4,"eligibilityCriteria":49,"healthyVolunteers":11,"sex":15,"minAge":50,"maxAge":51,"enrollmentInfo":52,"targetDuration":4,"studyType":20,"phases":54,"briefSummary":55,"conditions":56,"keywords":4,"overallStatus":58,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":59,"startDateStruct":60,"completionDateStruct":62,"leadSponsor":64,"locationsCount":5},"100554592","to-assess-the-utility-of-the-point-mini-in-a-clinical-take-home-study-100554592","NCT06501092","To Assess the Utility of the Point Mini in a Clinical Take-home Study","Inclusion Criteria:\n\n* Unilateral or bilateral partial hand limb differences\n* Fluent in English or Spanish\n* Ability to follow simple directions\n* Age between 3 and 17 years\n\nExclusion Criteria:\n\n* Patients with any unhealed wounds on their residual limb(s)\n* Significant cognitive deficits as determined upon clinical evaluation\n* Inability to follow simple directions\n* Significant physical deficits including pain and scarring impacting the design and fitting of the Point Mini prosthesis\n* Other psychosocial, personal, and medical co-morbidities expressed by the subject, family or study personnel","3 Years","17 Years",{"count":53,"type":19},14,[22],"The objective of this study is to evaluate the efficacy of the Point Mini system as compared to the subject's existing prosthetic treatment, which may include a prosthesis, other assistive device, or no device. This study will be a single subject crossover design where one group of 14 children with partial hand deficiencies will be evaluated on several metrics using their existing prosthetic treatment for one month and the Point Mini system for two months. Metrics include: in-clinic functional measures, subjective assessments, bilateral hand use, and prosthesis wear time.",[25,57],"Amputation, Congenital","RECRUITING",{"date":34,"type":35},{"date":61,"type":35},"2025-06-18",{"date":63,"type":19},"2027-07-31",{"name":41,"class":42},""]