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Differences in Outcomes and Failure Rates Between Allografts and Autografts in Revision Anterior Cruciate Ligament Reconstruction (ACLREV_GRAFT)

3 août 2026 mis à jour par: Stefano Zaffagnini

Anterior cruciate ligament (ACL) rupture is one of the most common knee injuries, particularly in young and physically active individuals. Despite advances in reconstruction techniques, graft failure and rerupture remain clinically relevant. Revision ACL surgery is more complex than primary reconstruction and is associated with inferior outcomes, with rerupture rates of approximately 13%, reaching up to 25% when both subjective and objective failure criteria are considered.

The main goal of ACL reconstruction is to restore anteroposterior and rotational knee stability, prevent secondary meniscal and cartilage damage, and enable return to sport. Surgical outcomes depend on several intraoperative factors, including graft choice and tunnel geometry, which are particularly relevant in revision settings.

Diagnosis of ACL rerupture is primarily clinical, based on instability tests (Lachman, anterior drawer, pivot shift), and supported by instrumental assessment such as the KT-1000 arthrometer, which provides an objective measure of joint laxity.

Revision ACL reconstruction can be performed using different surgical techniques (single-bundle, double-bundle, or combined extra-articular procedures) and graft types (autograft or allograft). Surgical strategy depends on multiple factors such as meniscal and cartilage status, previous surgery characteristics, tunnel positioning/enlargement, and fixation devices. However, no consensus exists regarding the optimal approach in terms of mid- to long-term outcomes.

A major long-term complication is the development of osteoarthritis, particularly in this typically young and active patient population. Identification of modifiable factors, such as surgical technique and graft type, may help reduce failure risk and joint degeneration.

This study aims to evaluate clinical and radiographic outcomes over a follow-up period exceeding two years in patients undergoing revision ACL reconstruction with different surgical techniques and graft types. The study also integrates objective knee laxity assessment using KT-1000 and markerless motion analysis based on artificial intelligence. Functional movements are recorded via video and analyzed using Sports2D software, enabling 2D kinematic analysis without markers or sensors, providing quantitative functional data to complement clinical and radiographic evaluation.

Aperçu de l'étude

Statut

Recrutement

Type d'étude

Observationnel

Inscription (Estimé)

150

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Lieux d'étude

    • Bologna
      • Bologna, Bologna, Italie, 40136
        • Recrutement
        • IRCCS Rizzoli Orthopedic Institute
        • Contact:

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte

Accepte les volontaires sains

Non

Méthode d'échantillonnage

Échantillon de probabilité

Population étudiée

Patients will be recruited among all subjects who underwent revision anterior cruciate ligament reconstruction at the SC Orthopaedic and Trauma Clinic II of the Istituto Ortopedico Rizzoli, with at least 2 years between the surgical procedure and the clinical-radiological reassessment proposed in this study, from 01/01/2016 to 31/12/2024 at the Istituto Ortopedico Rizzoli. Such reassessment is part of routine clinical practice.

La description

Inclusion Criteria:

  • Age 18-50 years at the time of surgery
  • Male and female patients
  • Patients undergoing revision anterior cruciate ligament (ACL) reconstruction with possible associated procedures, with at least 2 years of follow-up
  • Written informed consent to participate in the study

Exclusion criteria:

  • Patients lost to follow-up
  • Refusal to provide informed consent
  • Advanced knee osteoarthritis (Outerbridge grade III-IV) at the time of surgery
  • Severe obesity (BMI > 35)
  • Lower limb conditions preventing full weight-bearing standing during evaluation
  • Active infection, hematologic disease, or rheumatologic disease at the time of assessment

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Survival rate
Délai: At least 24 months after surgery
Failures will be recorded and documented in the case report form (CRF), during telephone questionnaires, and through the patient's clinical records (Electronic Health Record, SIR 2020, and hospital databases). The survival rate at follow-up will then be estimated using a Kaplan-Meier survival curve
At least 24 months after surgery

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Lysholm Knee Score
Délai: At least 24 months after surgery

It is a validated measurement scale that assesses knee function through 8 items, allowing evaluation of knee condition in relation to the functional demands of activities of daily living. This assessment form is used to evaluate surgical outcomes in patients undergoing surgery for ligamentous or meniscal knee injuries.

The final score is obtained by summing the scores of the individual items and ranges from 0 to 100. Scores are categorized into subgroups as follows: Excellent (95-100); Good (84-94); Fair (65-83); Poor (<64)

At least 24 months after surgery
International Knee Documentation Committee - Objective Knee Evaluation Form
Délai: At least 24 months after surgery

The objective IKDC is a clinical assessment form completed by the investigator, which allows standardized classification of knee status through objective parameters. The evaluation is based on four main domains: joint effusion, range of motion, ligament stability (in particular Lachman test, pivot-shift test, and anterior/posterior drawer tests), and joint compartments (meniscal and ligament examination).

The final outcome is not expressed as a continuous numerical score, but rather as a classification into four categories:

A (Normal) B (Nearly normal) C (Abnormal) D (Severely abnormal)

The final classification corresponds to the worst score obtained among the evaluated domains.

At least 24 months after surgery
Anterior drawer test
Délai: At least 24 months after surgery
It allows assessment of anterior tibial translation relative to the femur with the knee flexed at 90 degrees. An increased translation suggests a lesion of the reconstructed ACL (neo-ACL). It is graded on a scale from 0 to 3
At least 24 months after surgery
Lachman test
Délai: At least 24 months after surgery
It allows assessment of anterior tibial translation relative to the femur with the knee flexed at 30 degrees. Increased translation suggests a lesion of the reconstructed ACL (neo-ACL). It is graded on a scale from 0 to 3
At least 24 months after surgery
Pivot shift test
Délai: At least 24 months after surgery
This is a clinical examination maneuver used to assess rotational instability of the knee. The test is performed by applying a valgus and internal rotation stress during knee flexion; the occurrence of a tibial "shift" or "clunk" suggests a lesion of the reconstructed ACL (neo-ACL) associated with rotational instability. It is graded on a scale from 0 to 3.
At least 24 months after surgery
Tegner Activity Scale
Délai: At least 24 months after surgery

The Tegner Score is a physical activity rating scale that measures the level of participation in occupational and sports activities. The score ranges from 0 to 10, where:

0 indicates inability to work or severe disability due to knee problems;

10 indicates participation in competitive sports at national or international level (e.g., professional football).

Intermediate levels describe progressively more demanding physical activities, distinguishing between activities of daily living, light or heavy work, and recreational or competitive sports.

The Tegner Score is frequently used in combination with other instruments (such as the IKDC or Lysholm scores) to define the patient's functional level before injury and after treatment. In the context of this study, the score is collected through a direct patient interview conducted by the investigator.

At least 24 months after surgery
WOMAC
Délai: At least 24 months after surgery

The WOMAC (Western Ontario and McMaster Universities Osteoarthritis Index) is a self-administered questionnaire specifically developed to assess patients with hip and knee osteoarthritis. The instrument evaluates the impact of the disease on pain, stiffness, and physical function.

The questionnaire consists of 24 items divided into three main domains:

  • Pain (5 items)
  • Joint stiffness (2 items)
  • Physical function (17 items)

The total score is normalized on a 0-100 scale.

At least 24 months after surgery
KT-1000
Délai: At least 24 months after surgery
The KT-1000 is an objective assessment device that measures anterior tibial translation relative to the femur by applying a predefined force to translate the tibia anteriorly. Its use is part of routine clinical practice in the outpatient setting of the Second Orthopaedic and Trauma Clinic of the IOR and aims to quantitatively assess static anteroposterior knee laxity following anterior cruciate ligament reconstruction. The unit of measurement is millimetres
At least 24 months after surgery
Post-operative movement analysis
Délai: At least 24 months after surgery

Knee function will be assessed during functional tasks (walking, lunges, squat) using a markerless AI-based video analysis system (Sports2D). The software estimates 2D joint kinematics (hip, knee, ankle, trunk) from videos recorded in frontal and sagittal planes without the use of sensors or markers. The system is non-invasive, already used in clinical practice, and installed locally to ensure data protection.

Videos are processed through an internal MATLAB script that extracts kinematic outputs (.mot and .trc files) using automated AI-based analysis. Data are anonymized via alphanumeric IDs, and videos are deleted after processing to minimize data retention.

At least 24 months after surgery

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Parrainer

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

8 juillet 2026

Achèvement primaire (Estimé)

1 mai 2027

Achèvement de l'étude (Estimé)

1 mai 2027

Dates d'inscription aux études

Première soumission

22 juin 2026

Première soumission répondant aux critères de contrôle qualité

22 juin 2026

Première publication (Réel)

26 juin 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

4 août 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

3 août 2026

Dernière vérification

1 août 2026

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • ACLREV_GRAFT

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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