The Effect of Knee Flexion Angle for Graft Fixation During Single-Bundle Anterior Cruciate Ligament Reconstruction (KFA-FIRM)
Anterior Cruciate Ligament Injury
About this trial
This is an interventional treatment trial for Anterior Cruciate Ligament Injury focused on measuring ACL, ACL reconstruction, Knee Flexion Angle, Bone Patellar Tendon Bone
Eligibility Criteria
Inclusion Criteria:
- Male and female patients older than 16 years old with an isolated anterior cruciate ligament injury as diagnosed by clinical examination and MRI
- No pre-existing arthritis as defined by the Kellgren-Lawrence radiographic rating system
- Patients treated with an initial period of rehabilitation to eliminate swelling, optimize quadriceps strength and restore range of motion
- Surgical management with a transtibial or anteromedial portal single-bundle ACLR with bone patella tendon bone (BPTB) autograft by a fellowship-trained sports medicine surgeon.
- Provision of Informed Consent
Exclusion Criteria:
- Acute ACL injuries that have not undergone an initial period of physical therapy in order to restore the aforementioned parameters
- Associated grade III injury to the MCL (medial opening >10mm at 30 degrees of knee flexion or any medial opening in extension);
- Presence of a PCL or posterolateral corner injury
- Lack of informed consent.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
0 degree Knee Flexion Angle ACLR
30 degree Knee Flexion Angle ACLR
At the time of surgery, tunnel position and surgical technique will be standardized for transtibial and anteromedial portal ACLR. Individuals randomized to this arm intra-operatively to undergo fixation of the ACL graft on the tibial side at a KFA of 0 degrees as measured by a sterile goniometer. Grafts will be tensioned according to the maximum surgeon-applied tension at the designated KFA. After surgery, patients will be treated with a standardized accelerated physical therapy protocol
At the time of surgery, tunnel position and surgical technique will be standardized for transtibial and anteromedial portal ACLR. Individuals randomized to this arm intra-operatively to undergo fixation of the ACL graft on the tibial side at a KFA of 30 degrees as measured by a sterile goniometer. Grafts will be tensioned according to the maximum surgeon-applied tension at the designated KFA. After surgery, patients will be treated with a standardized accelerated physical therapy protocol