ACL Reconstruction: Clinical Outcome

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.

Inclusion Criteria: 1. Patients who have provided informed written written consent; 2. Patients aged between 18 and 60; 3. Patients undergoing reconstructive surgical treatment of the anterior cruciate ligament (ACL) Exclusion Criteria: 1. Patients unable to understand and to want; 2. Patients who have not signed informed consent;