Degenerative Lesion of Articular Cartilage of Knee Clinical Trial
Official title:
Tissue Engineered Nasal Cartilage for Regeneration of Articular Cartilage in the Knee After Traumatic Injury - a Phase I Clinical Trial-
The purpose of this study is to investigate the safety and feasibility of implanting an engineered cartilage graft obtained by culturing expanded autologous nasal chondrocytes within a collagen type I/III membrane into the cartilage defect on the femoral condyle and/or trochlea of the knee after a traumatic injury.
Articular cartilage injuries are a prime target for regenerative techniques, since
spontaneous healing is poor and untreated defects predispose to osteoarthritis. Common
current strategies such as arthroscopic debridement, microfracture, autologous osteochondral
grafting, use of allografts and autologous chondrocytes implantation (ACI) still have
drawbacks such as long and complex rehabilitation times, technically challenging operation
techniques, defect-size limitations, donor-site morbidity, limited graft material and high
costs. Furthermore many techniques show unsatisfactory long term results due to inferior
quality of repair tissue as compared to native cartilage or have yet to prove the cost versus
benefit. These drawbacks could be overcome by using a tissue engineered nasal cartilage
graft, thereby reducing donor site morbidity without introducing additional risk of
complication or technically challenging techniques.
This study is a phase I, prospective, uncontrolled, investigator initiated clinical trial
involving 25 patients, with the objective of demonstrating safety and feasibility in the use
of engineered nasal cartilage grafts for repair of articular cartilage. The specific surgical
target of the trial is the repair of one or two full-thickness cartilage defects from 2 cm2
to 8 cm2 (per lesion, not exceeding a total of 8 cm2 for all lesions) due to traumatic injury
on the femoral condyle and/or trochlea of the knee.
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