ACL Reconstruction: Clinical Outcome
Condition(s) studied
Investigational drug(s) / intervention(s)
ACL reconstruction: Surgical ACL reconstruction
Study 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
Primary outcome measure(s)
- Knee Laxity Assessment — 5 years
Laxity Evaluation with KiRA device
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Stefano Zaffagnini | Bologna | Italia | Recruiting |
More Stefano Zaffagnini trials in Italy
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT03441659 on ClinicalTrials.gov ↗ ← All trials in Italy