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Not Yet Recruiting NCT07935512

Clinical and Instrumental Assessment and Evaluation of Return to Sport in Patients Who Underwent Surgical Treatment for Posterolateral Corner (PLC) Injuries Associated With Anterior Cruciate Ligament (ACL) Injuries.

Conditions: Anterior Cruciate Ligament (ACL), Posterolateral Corner

Sex: All
Ages: 18 Years – 65 Years
Healthy volunteers: No
Enrollment: 16
Sponsor: Stefano Zaffagnini

Location: IRCCS Rizzoli Orthopedic Institute Bologna Bologna

Summary

This is a single-centre, observational retrospective and prospective study aimed at evaluating the clinical and functional outcomes of patients who underwent combined anterior cruciate ligament (ACL) and posterolateral corner (PLC) reconstruction using the Over-The-Top (OTT) technique. The primary outcome is the improvement in knee function, assessed using the Lysholm Knee Score by comparing pre-injury/preoperative status with postoperative follow-up. Secondary outcomes include knee stability, assessed through clinical examinations and instrumental measurements (KT-1000, KiRA, PIVOT App and Telos stress radiographs), return to sport, pain, MRI findings and postoperative complications. Patients aged 18-65 years with a minimum follow-up of 24 months will be included. The study aims to provide evidence on the effectiveness of the combined ACL and PLC reconstruction using the OTT technique.

Eligibility Criteria

Inclusion Criteria * Male and female patients; * Patients aged between 18 and 65 years at the time of surgery; * Patients who underwent anterior cruciate ligament (ACL) reconstruction using the Over-The-Top (OTT) technique combined with posterolateral corner (PLC) reconstruction; * Patients who underwent surgery between January 1, 2017, and December 31, 2025; * Patients who underwent preoperative imaging examinations (MRI and, if applicable, X-rays) of the affected knee confirming the diagnosis of ACL and posterolateral corner injuries; * Patients who underwent isolated ACL + PLC reconstruction or ACL + PLC reconstruction combined with additional procedures on the same knee (e.g., meniscal treatment or concomitant ligament injuries); * Patients who provided written informed consent to participate in the study. Exclusion Criteria * History of fractures of the same limb requiring surgical treatment; * History of posterolateral corner (PLC) injuries of the knee requiring surgical treatment; * Patients younger than 18 years or older than 65 years at the time of surgery; * Patients who did not provide informed consent; * Patients who are no longer contactable.

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07935512). StuddyBuddy aggregates publicly available trial information.