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BioPoly RS Knee Registry Study for Cartilage Defect Replacement

Cartilage Injury Clinical Trial

Official title:
Multi-centre, Open Label, Prospective, Consecutive Series Registry Database of BioPoly RS Partial Resurfacing Knee Implant

Clinical Trial Summary

Information will be collected on the pre-op and post-op clinical status of patients with focal cartilage defects of the femoral condyles treated with the BioPoly RS Partial Resurfacing Knee Implant, a permanent orthopaedic implant. The overall aim of the study is to increase the knowledge of patient outcomes such as pain, knee function, level of activity, and overall quality of life after treatment with the device.

Clinical Trial Description

Information will be collected on the pre-op and post-op clinical status of patients with focal cartilage defects of the femoral condyles treated with the BioPoly RS Partial Resurfacing Knee Implant, a permanent orthopaedic implant. The overall aim of the study is to increase the knowledge of patient outcomes such as pain, knee function, level of activity, and overall quality of life after treatment with the device. Patients will be followed for 5 years after surgery. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01473199
Study type Interventional
Source BioPoly LLC
Contact
Status Completed
Phase N/A
Start date November 2011
Completion date December 2021
View Details
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