ACL Reconstruction: Clinical Outcome

ConditionACL Injury
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-60
SponsorStefano Zaffagnini

About this trial

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.

Eligibility criteria

Qualifiers

Patients who have provided informed written written consent;

Patients aged between 18 and 60;

Patients undergoing reconstructive surgical treatment of the anterior cruciate ligament (ACL)

Disqualifiers

Patients unable to understand and to want;

Patients who have not signed informed consent;

Trial design

Treatments tested in this trial

  • ACL reconstruction

Treatment groups

No treatment groups listed

Locations

1
Stefano Zaffagnini BolognaItalia, Italy

Sponsors and collaborators

Stefano Zaffagnini

Lead sponsor

Istituto Ortopedico Rizzoli

Sponsor institution