[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100319659":3},{"organization":4,"armGroups":7,"interventions":8,"overallOfficials":7,"centralContacts":13,"locations":24,"responsibleParty":42,"collaborators":7,"id":45,"slug":46,"hasResults":47,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":51,"eligibilityCriteria":52,"healthyVolunteers":47,"sex":53,"minAge":54,"maxAge":55,"enrollmentInfo":56,"targetDuration":7,"studyType":59,"phases":7,"briefSummary":60,"conditions":61,"keywords":7,"overallStatus":27,"whyStopped":7,"lastUpdateSubmitDate":63,"lastUpdatePostDateStruct":64,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":71,"locationsCount":72},{"fullName":5,"class":6},"Istituto Ortopedico Rizzoli","OTHER",null,[9],{"type":10,"name":11,"description":12,"armGroupLabels":7,"otherNames":7},"PROCEDURE","ACL reconstruction","Surgical ACL reconstruction",[14,19],{"name":15,"role":16,"phone":17,"phoneExt":7,"email":18},"Stefano Zaffagnini, MD","CONTACT","0516366567","stefano.zaffagnini@ior.it",{"name":20,"role":16,"phone":21,"phoneExt":22,"email":23},"Roberta Licciardi, MD","6366567","051","roberta.licciardi@ior.it",[25],{"facility":26,"status":27,"city":28,"state":29,"zip":7,"country":30,"countryCode":31,"cosmosGeoPoint":32,"geoPoint":37,"contacts":38},"Stefano Zaffagnini","RECRUITING","Bologna","Italia","Italy","IT",{"type":33,"coordinates":34},"Point",[35,36],11.33875,44.49381,{"lat":36,"lon":35},[39],{"name":15,"role":16,"phone":40,"phoneExt":7,"email":41},"051 6366075","stefano.zaffagnini@unibo.it",{"type":43,"investigatorFullName":26,"investigatorTitle":44,"investigatorAffiliation":5,"oldNameTitle":7,"oldOrganization":7},"SPONSOR_INVESTIGATOR","Prof","100319659","acl-reconstruction-clinical-outcome-100319659",false,"NCT03441659","ACL Reconstruction: Clinical Outcome","Anterior Cruciate Ligament Reconstruction: Clinical Outcome at Middle and Long Term Follow-Up","RIC-ACL","Inclusion Criteria:\n\n1. Patients who have provided informed written written consent;\n2. Patients aged between 18 and 60;\n3. Patients undergoing reconstructive surgical treatment of the anterior cruciate ligament (ACL)\n\nExclusion Criteria:\n\n1. Patients unable to understand and to want;\n2. Patients who have not signed informed consent;","ALL","18 Years","60 Years",{"count":57,"type":58},1000,"ESTIMATED","OBSERVATIONAL","The study is intended to include all patients who will undergo surgical reconstruction of the anterior cruciate ligament (ACL). The patients will be monitored and evaluated preoperatively and also at 6 months and 1, 2 and 5 years after the intervention through a clinical visit or telephone interview. Such assessments will include the administration of questionnaires to determine the patient's functional symptoms and the objective examination of the knee during a medical examination to quantify its stability.",[62],"ACL Injury","2026-01-29",{"date":65,"type":66},"2026-02-02","ACTUAL",{"date":68,"type":66},"2020-12-17",{"date":70,"type":58},"2030-12",{"name":26,"class":6},1]