ACL Reconstruction: Clinical Outcome

Recruiting now

Conditions studied: ACL Injury

In brief

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.

Key facts

Study ID

NCT03441659

Run by

Stefano Zaffagnini

People needed

1000

Starts

2020-12-17

Expected to finish

2030-12-01

Last updated by the study team

2026-07-09

Who can join

Age: 18 and older, up to 60. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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)

You may not qualify if…

• Patients unable to understand and to want;
• Patients who have not signed informed consent;

Where it is running

• Stefano Zaffagnini — Bologna, Italia, Italy (enrolling)

Full record on ClinicalTrials.gov

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