[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100358151":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":28,"centralContacts":11,"locations":33,"responsibleParty":46,"collaborators":11,"id":48,"slug":49,"hasResults":50,"nctId":51,"briefTitle":52,"officialTitle":52,"acronym":11,"eligibilityCriteria":53,"healthyVolunteers":50,"sex":54,"minAge":55,"maxAge":11,"enrollmentInfo":56,"targetDuration":11,"studyType":59,"phases":60,"briefSummary":62,"conditions":63,"keywords":11,"overallStatus":66,"whyStopped":11,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":75},{"fullName":5,"class":6},"NYU Langone Health","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Standard of Care","ACTIVE_COMPARATOR",null,[13],"Procedure: Standard of Care",{"label":15,"type":16,"description":11,"interventionNames":17},"Distal Targeting Treatment","EXPERIMENTAL",[18],"Procedure: Distal targeting device technique of distal screw placement",[20,24],{"type":21,"name":9,"description":22,"armGroupLabels":23,"otherNames":11},"PROCEDURE","Will receive the standard of care \"free-hand\" technique of distal screw placement, as treated by Dr. Egol or Dr. Tejwani.",[9],{"type":21,"name":25,"description":26,"armGroupLabels":27,"otherNames":11},"Distal targeting device technique of distal screw placement","The second group will be the interventional group which will use the distal targeting device technique of distal screw placement and will be treated by Dr. Konda and Dr. Leucht. All relevant data to the study will be collected intra-operatively.",[15],[29],{"name":30,"affiliation":31,"role":32},"Sanjit Konda, MD","New York Langone Medical Center","PRINCIPAL_INVESTIGATOR",[34],{"facility":35,"status":11,"city":36,"state":36,"zip":37,"country":38,"countryCode":39,"cosmosGeoPoint":40,"geoPoint":45,"contacts":11},"New York University School of Medicine","New York","10016","United States","US",{"type":41,"coordinates":42},"Point",[43,44],-74.00597,40.71427,{"lat":44,"lon":43},{"type":47,"investigatorFullName":11,"investigatorTitle":11,"investigatorAffiliation":11,"oldNameTitle":11,"oldOrganization":11},"SPONSOR","100358151","trial-of-a-distal-targeting-system-for-cephalomedullary-nails-as-part-of-surgical-repair-of-hip-and-femoral-shaft-fractures-100358151",false,"NCT03943329","Trial of a Distal Targeting System for Cephalomedullary Nails as Part of Surgical Repair of Hip and Femoral Shaft Fractures","Inclusion Criteria:\n\n* The patient must be greater than or equal to 18 years of age.\n* The patient must have sustained a hip or femur fracture that is indicated for cephalomedullary nailing as the primary and definitive treatment measure.\n* The patient must be medically cleared for operative fixation of their fracture.\n\nExclusion Criteria:\n\n* The patient does not meet all of the inclusion criteria.","ALL","18 Years",{"count":57,"type":58},60,"ACTUAL","INTERVENTIONAL",[61],"NA","This study will be a prospective, case - control trial looking at the use of a previously FDA approved device made by Stryker, a distal targeting system that eases the distal targeting of screws in cephalomedullary nails in hip and femoral shaft fractures. Patients who consent to participate in the study will either be in the control or device arm of the study depending on their surgeon.",[64,65],"Hip Fractures","Femoral Shaft Fractures","COMPLETED","2022-02-10",{"date":69,"type":58},"2022-02-14",{"date":71,"type":58},"2019-12-17",{"date":73,"type":58},"2021-03-07",{"name":5,"class":6},1]