[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100418138":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":26,"centralContacts":34,"locations":41,"responsibleParty":55,"collaborators":25,"id":58,"slug":59,"hasResults":60,"nctId":61,"briefTitle":62,"officialTitle":63,"acronym":25,"eligibilityCriteria":64,"healthyVolunteers":65,"sex":66,"minAge":67,"maxAge":25,"enrollmentInfo":68,"targetDuration":25,"studyType":71,"phases":72,"briefSummary":74,"conditions":75,"keywords":77,"overallStatus":81,"whyStopped":25,"lastUpdateSubmitDate":82,"lastUpdatePostDateStruct":83,"startDateStruct":86,"completionDateStruct":88,"leadSponsor":90,"locationsCount":91},{"fullName":5,"class":6},"Hospital District of Helsinki and Uusimaa","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Weight-bearing as tolerated","EXPERIMENTAL","Patients are instructed to mobilise the hip and weight-bear as tolerated",[13],"Procedure: Open reduction and internal fixation (ORIF)",{"label":15,"type":16,"description":17,"interventionNames":18},"Touch-down weight-bearing","ACTIVE_COMPARATOR","Patients are instructed to mobilise the hip. Touch-down weight-bearing for 6-8 weeks",[13],[20],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":25},"PROCEDURE","Open reduction and internal fixation (ORIF)","Approaches used:\n\n* Intrapelvic approach +\u002F- iliac window\n* Kocher-Langenbeck approach",[15,9],null,[27,31],{"name":28,"affiliation":29,"role":30},"Jan Lindahl, MD, PhD","Helsinki University Central Hospital","STUDY_CHAIR",{"name":32,"affiliation":29,"role":33},"Kristian Seppänen, MD","PRINCIPAL_INVESTIGATOR",[35,39],{"name":32,"role":36,"phone":37,"phoneExt":25,"email":38},"CONTACT","094711","kristian.seppanen@hus.fi",{"name":28,"role":36,"phone":37,"phoneExt":25,"email":40},"jan.lindahl@hus.fi",[42],{"facility":43,"status":25,"city":44,"state":45,"zip":46,"country":47,"countryCode":48,"cosmosGeoPoint":49,"geoPoint":54,"contacts":25},"Helsinki University Hospital","Helsinki","Uusimaa","00029 HUS","Finland","FI",{"type":50,"coordinates":51},"Point",[52,53],24.93545,60.16952,{"lat":53,"lon":52},{"type":33,"investigatorFullName":56,"investigatorTitle":57,"investigatorAffiliation":5,"oldNameTitle":25,"oldOrganization":25},"Kristian Seppänen","Principal Investigator","100418138","weight-bearing-of-surgically-treated-acetabular-fractures-100418138",false,"NCT04724811","Weight-bearing of Surgically Treated Acetabular Fractures.","Weight-bearing of Surgically Treated Acetabular Fractures. A Randomised Controlled Trial","Inclusion Criteria:\n\n* Unilateral dislocated acetabulum fracture (displacement of over 2mm in preoperative CT scan)\n* The osteosynthesis is performed during 21 days after initial trauma\n* The patient is willing to participate in the follow-up\n\nExclusion Criteria:\n\n* Unwillingness to participate in randomisation\n* Bilateral fracture\n* Letournel \\& Judet type Both column or Posterior column and wall fractures\n* Any other injury that prevents the patient from partial weight bearing\n* Open fracture of the acetabulum\n* Pathologic fracture (fragility fractures are not an exclusion criteria)\n* Prior functional disability in the pelvis or lower extremity\n* Non-Compliance due to dementia or other mental disability\n* Prior daily pain medication due to hip-pain\n* Unwillingness to accept one of the two mobilisation protocols\n* Prior hip replacement on injured side\n* BMI \\> 40",true,"ALL","60 Years",{"count":69,"type":70},50,"ESTIMATED","INTERVENTIONAL",[73],"NA","The purpose of this study is to determine whether patients with operatively treated acetabular fractures benefit from early weight-bearing as tolerated. The study compares two groups ( n = 25 each), which are randomised into either weight-bearing as tolerated or touch-down weight-bearing for 6-8 weeks postoperatively.\n\nBoth study groups are stratified according to\n\n* Type of fracture (anterior approach vs anterior + additional posterior approach)\n* Dislocated dome vs non-dislocated\u002F non existing separate dome fragment\n\nPatients, who are eligible to participate in the trial but choose not to participate in randomisation are asked to enrol in a prospective cohort follow-up cohort. This is to examine a potential participation bias in the RCT groups. These patients will not be counted into the target amount of 50 RCT patients.",[76],"Acetabular Fracture",[78,79,80],"Acetabulum","Periarticular fracture","Weight-bearing","NOT_YET_RECRUITING","2024-03-05",{"date":84,"type":85},"2024-03-06","ACTUAL",{"date":87,"type":70},"2024-05",{"date":89,"type":70},"2027-12",{"name":5,"class":6},1]