ACL Injury Clinical Trial
Official title:
Randomized Controlled Trial for the Use of an Osteoconductive Scaffold in ACL-Reconstruction
Primary objective of the study is to evaluate efficacy of the surgical technique for ACL reconstruction using an osteoconductive scaffold, enlaced into the hamstring tendon autograft, compared to the traditional technique.
Reconstruction of the anterior cruciate ligament (ACL) using autograft tissue is currently
recommended as the standard of care following an ACL tear or rupture, with the
bone-tendon-bone (BTB) graft and hamstring tendon graft the most common. Although a BTB
autograft is widely recognized to offer high mechanical performance and rapid graft healing,
these advantages come at the cost of a longer surgery time and higher risk of severe patient
discomfort at the graft harvest site. Use of a hamstring tendon autograft is less painful,
but is generally slower to heal with higher risk of mechanical graft failure due to poor bone
ingrowth. The aim of the current study is to augment graft-to-bone incorporation by use of an
osteoconductive scaffold enlaced into the hamstring tendon autograft. This bovine derived
composite bone substitute is inserted into the articular aperture of the femoral bone tunnel
and should provide an osteoconductive / osteoinductive environment at a biomimetic attachment
site leading to improved secondary graft-fixation and a reduced incidence of tunnel widening.
Primary objective of the study is to evaluate efficacy of the surgical technique for ACL
reconstruction using an osteoconductive scaffold, enlaced into the hamstring tendon
autograft, compared to the traditional technique.
Secondary objectives aim to assess the clinical outcome of the interventional treatment
including patient subjective knee function and objective measures of knee stability.
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