[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100174187":3},{"organization":4,"armGroups":7,"interventions":8,"overallOfficials":7,"centralContacts":7,"locations":13,"responsibleParty":26,"collaborators":7,"id":28,"slug":29,"hasResults":30,"nctId":31,"briefTitle":32,"officialTitle":7,"acronym":7,"eligibilityCriteria":33,"healthyVolunteers":30,"sex":34,"minAge":35,"maxAge":36,"enrollmentInfo":37,"targetDuration":7,"studyType":40,"phases":41,"briefSummary":44,"conditions":45,"keywords":7,"overallStatus":47,"whyStopped":7,"lastUpdateSubmitDate":48,"lastUpdatePostDateStruct":49,"startDateStruct":52,"completionDateStruct":7,"leadSponsor":54,"locationsCount":55},{"fullName":5,"class":6},"Vascutek Ltd.","INDUSTRY",null,[9],{"type":10,"name":11,"description":12,"armGroupLabels":7,"otherNames":7},"DEVICE","Vascutek Hybrid Graft","Single Group Assignment",[14],{"facility":15,"status":7,"city":16,"state":7,"zip":17,"country":18,"countryCode":19,"cosmosGeoPoint":20,"geoPoint":25,"contacts":7},"Division of Thoracic and Cardiovascular Surgery, Hannover Medical School","Hanover","30625","Germany","DE",{"type":21,"coordinates":22},"Point",[23,24],9.73322,52.37052,{"lat":24,"lon":23},{"type":27,"investigatorFullName":7,"investigatorTitle":7,"investigatorAffiliation":7,"oldNameTitle":7,"oldOrganization":7},"SPONSOR","100174187","phase-1-evaluation-of-the-vascutek-hybrid-graft-for-use-in-the-replacement-of-the-aortic-arch-and-concomitant-treatment-of-an-aneurysmdissection-of-the-descending-aorta-in-the-frozen-elephant-trunk-procedure-100174187",false,"NCT01541410","Evaluation of the Vascutek Hybrid Graft for Use in the Replacement of the Aortic Arch and Concomitant Treatment of an Aneurysm\u002FDissection of the Descending Aorta in the Frozen Elephant Trunk Procedure","Inclusion Criteria:\n\n1. Patients with aneurysm and\u002For dissection of the aortic arch and\u002For descending aorta\n2. Patient must have agreed to participate voluntarily and have signed and dated an Ethics Committee approved Patient Informed Consent\n3. Patient is able and willing to comply with the protocol and associated follow-up requirements\n\nExclusion Criteria:\n\n1. Patients unfit for open surgical repair involving circulatory arrest\n2. Endocarditis or active infective disorder of the aorta\n3. Patients unwilling to give informed consent","ALL","29 Years","79 Years",{"count":38,"type":39},34,"ACTUAL","INTERVENTIONAL",[42,43],"PHASE1","PHASE2","The purpose of this feasibility study is to investigate the clinical performance of the Vascutek Hybrid Device in the treatment of subjects with aneurysm and\u002For dissection of the thoracic aorta.",[46],"Aneurysmal Disease of the Ascending Aorta, the Arch and the Proximal Descending Aorta","COMPLETED","2013-07-12",{"date":50,"type":51},"2013-07-15","ESTIMATED",{"date":53,"type":7},"2010-05",{"name":5,"class":6},1]