Ireland
--:--IST
Latest
Recruiting Observational

ACL Reconstruction: Clinical Outcome

NCT03441659 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2020-12-17
Last updated
2026-07-09

Condition(s) studied

ACL Injury

Investigational drug(s) / intervention(s)

ACL reconstruction

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

Sex
ALL
Min age
18 Years
Max age
60 Years
Healthy volunteers
No
Inclusion Criteria: 1. Patients who have provided informed written written consent; 2. Patients aged between 18 and 60; 3. Patients undergoing reconstructive surgical treatment of the anterior cruciate ligament (ACL) Exclusion Criteria: 1. Patients unable to understand and to want; 2. Patients who have not signed informed consent;

Primary outcome measure(s)

  • Knee Laxity Assessment — 5 years
    Laxity Evaluation with KiRA device

Trial sites (1)

FacilityCityRegionStatus
Stefano Zaffagnini Bologna Italia Recruiting
Official registry record

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