[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100543824":3},{"organization":4,"armGroups":7,"interventions":24,"overallOfficials":37,"centralContacts":42,"locations":51,"responsibleParty":67,"collaborators":10,"id":70,"slug":71,"hasResults":72,"nctId":73,"briefTitle":74,"officialTitle":75,"acronym":10,"eligibilityCriteria":76,"healthyVolunteers":72,"sex":77,"minAge":78,"maxAge":10,"enrollmentInfo":79,"targetDuration":82,"studyType":83,"phases":10,"briefSummary":84,"conditions":85,"keywords":10,"overallStatus":87,"whyStopped":10,"lastUpdateSubmitDate":88,"lastUpdatePostDateStruct":89,"startDateStruct":92,"completionDateStruct":94,"leadSponsor":96,"locationsCount":97},{"fullName":5,"class":6},"Regional Hospital of Bolzano","OTHER",[8,14,19],{"label":9,"type":10,"description":11,"interventionNames":12},"Conservative",null,"Participants allocated to conservative management will receive an orthosis (Gilchrist) for a minimum of four weeks. Using Gilchrist, the upper arm of the injured side is secured in abduction and internal rotation with the weight of the arm held by a ring around the patient's neck. At four weeks, plain radiographs of the shoulder will be conducted to ascertain the presence of the bony callous. If a bony callous is not present, the patient will maintain Gilchrist and plain radiographs of the shoulder will be conducted on a biweekly basis until a bony callous will be evident. If a bony callous is present, the patient will start a structured program of rehabilitation.",[13],"Procedure: Conservative",{"label":15,"type":10,"description":16,"interventionNames":17},"Open Reduction Internal Fixation","Participants allocated to ORIF will undergo surgery within 72 hours from the diagnosis using a standard deltopectoral approach. An angular stable plate is used in all patients following manufacturer instructions. No drains will be used.",[18],"Procedure: ORIF",{"label":20,"type":10,"description":21,"interventionNames":22},"Closed Reduction Percutaneous Pinning","Participants allocated to CRPP will be positioned in a beach chair under total anesthesia. The fracture is repositioned under fluoroscopic guidance using manual traction. The osteosynthesis is then done using Kirschner wires.The arm is placed into a Gilchrist for four weeks. At four weeks, plain radiographs of the shoulder will be conducted to ascertain the presence of the bony callous. If a bony callous is not present, the patient will maintain Gilchrist and plain radiographs of the shoulder will be conducted on a biweekly basis until a bony callous will be evident. If a bony callous is present, the Kirschner wires will be removed and the patient will start a structured program of rehabilitation.",[23],"Procedure: CRPP",[25,29,33],{"type":26,"name":9,"description":27,"armGroupLabels":28,"otherNames":10},"PROCEDURE","Conservative treatment",[9],{"type":26,"name":30,"description":31,"armGroupLabels":32,"otherNames":10},"ORIF","Open surgery",[15],{"type":26,"name":34,"description":35,"armGroupLabels":36,"otherNames":10},"CRPP","Minimal invasive surgery",[20],[38],{"name":39,"affiliation":40,"role":41},"Filippo Migliorini, Dr.","employee","PRINCIPAL_INVESTIGATOR",[43,48],{"name":44,"role":45,"phone":46,"phoneExt":10,"email":47},"Malte Nikolas Witte, Dr.","CONTACT","00393885787726","maltewitte@posteo.de",{"name":39,"role":45,"phone":49,"phoneExt":10,"email":50},"00393278751794","migliorini.md@gmail.com",[52],{"facility":53,"status":10,"city":54,"state":55,"zip":56,"country":57,"countryCode":58,"cosmosGeoPoint":59,"geoPoint":64,"contacts":65},"Academic Hospital of Bolzano (SABES-ASDAA)","Bolzano","Trentino-Alto Adige","39100","Italy","IT",{"type":60,"coordinates":61},"Point",[62,63],11.33982,46.49067,{"lat":63,"lon":62},[66],{"name":44,"role":45,"phone":46,"phoneExt":10,"email":47},{"type":41,"investigatorFullName":68,"investigatorTitle":69,"investigatorAffiliation":5,"oldNameTitle":10,"oldOrganization":10},"Malte Nikolas Witte","Medical Doctor","100543824","management-of-proximal-humerus-fractures-in-adults-a-clinical-trial-100543824",false,"NCT06360887","Management of Proximal Humerus Fractures in Adults: a Clinical Trial","Management of Proximal Humerus Fractures in Elderlies: a Clinical Trial","Inclusion Criteria:\n\n1. adults who sustained a Proximal Humerus Fracture within the last week\n2. type of Proximal Humerus Fracture AO 11-(A2, A3), 11- (B1, B2, B3)\n3. BMI lower than 40 Kg\u002Fm2\n\nExclusion Criteria:\n\n1. stress fractures\n2. revision setting\n3. open fractures\n4. fractures associated with a neurologic lesion; previous fractures or bony procedure at the homolateral side\n5. patients unable to understand the procedure or instructions for rehabilitation\n6. terminal patients\n7. patients presenting multiple injuries","ALL","18 Years",{"count":80,"type":81},351,"ESTIMATED","2 Years","OBSERVATIONAL","Prospective patient registry examining the outcome of three different treatment methods for proximal humerus fractures in elderlies: conservative treatment, open and minimal invasive surgical treatment.",[86],"Shoulder Fractures","NOT_YET_RECRUITING","2024-04-10",{"date":90,"type":91},"2024-04-12","ACTUAL",{"date":93,"type":81},"2024-04",{"date":95,"type":81},"2028-01-31",{"name":5,"class":6},1]