[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100319659":3},{"organization":4,"armGroups":7,"interventions":8,"overallOfficials":7,"centralContacts":13,"locations":24,"responsibleParty":41,"collaborators":7,"id":44,"slug":7,"hasResults":45,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":49,"eligibilityCriteria":50,"healthyVolunteers":45,"sex":51,"minAge":52,"maxAge":53,"enrollmentInfo":54,"targetDuration":7,"studyType":57,"phases":7,"briefSummary":58,"conditions":59,"keywords":7,"overallStatus":27,"whyStopped":7,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":70},{"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,"cosmosGeoPoint":31,"geoPoint":36,"contacts":37},"Stefano Zaffagnini","RECRUITING","Bologna","Italia","Italy",{"type":32,"coordinates":33},"Point",[34,35],11.33875,44.49381,{"lat":35,"lon":34},[38],{"name":15,"role":16,"phone":39,"phoneExt":7,"email":40},"051 6366075","stefano.zaffagnini@unibo.it",{"type":42,"investigatorFullName":26,"investigatorTitle":43,"investigatorAffiliation":5,"oldNameTitle":7,"oldOrganization":7},"SPONSOR_INVESTIGATOR","Prof","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":55,"type":56},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.",[60],"ACL Injury","2026-01-29",{"date":63,"type":64},"2026-02-02","ACTUAL",{"date":66,"type":64},"2020-12-17",{"date":68,"type":56},"2030-12",{"name":26,"class":6},1]