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Clinical Trial Summary

The purpose of this study is to assess safety and efficacy of autologous chondrocyte implantation delivered arthroscopically into chondral lesions of the knee using clinical, biochemical, and MRI outcomes.


Clinical Trial Description

Injuries to the articular cartilage of the knee are common. They produce pain and deteriotation of patients' quality of life. The management of focal chondral lesions continues to be problematic for the treating orthopaedic surgeon. Although many treatment options are currently available, none fulfill the criteria for an ideal repair solution: a hyaline repair tissue that completely fills the defect and integrates well with the surrounding normal cartilage. Autologous chondrocyte implantation is a relatively new cell-based treatment method for full-thickness cartilage injuries that in recent years has increased in popularity, with different studies showing promising results. Typically, this implantation is performed in an open-surgery fashion. In our study the implantation of in-house autologous chondrocyte culture is done arthroscopically, situation that may offer advantages in surgery associated morbidity and patient recovery. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01503970
Study type Interventional
Source Instituto Nacional de Rehabilitacion
Contact
Status Completed
Phase Phase 1/Phase 2
Start date December 2008
Completion date December 2012

See also
  Status Clinical Trial Phase
Completed NCT02673905 - Clinical Trial for the Regeneration of Cartilage Lesions in the Knee N/A
Completed NCT01947374 - Arthroscopic Autologous Chondrocyte Implantation Versus Microfractures Phase 3