ACL Reconstruction: Clinical Outcome
Anterior Cruciate Ligament Reconstruction: Clinical Outcome at Middle and Long Term Follow-Up
Stefano Zaffagnini
1,000 participants
Dec 17, 2020
OBSERVATIONAL
Conditions
Summary
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
Inclusion Criteria3
- 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)
Exclusion Criteria2
- Patients unable to understand and to want;
- Patients who have not signed informed consent;
Interested in this trial?
Get notified about updates and connect with the research team.
Interventions
Surgical ACL reconstruction
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT03441659