A Stratified, Post-Market Study of DeNovo NT for Treatment of Femoral and Patellar Articular Cartilage Lesions of the Knee
The purpose of this research study is to evaluate improvement in subject-reported clinical outcomes over a period of two (2) years following treatment of articularl cartilage lesions of the knee with DeNovo NT
Cartilage injury of the knee
Candidates must be between the ages of 18 and 55, and have diagnosed cartilage injury for which they are a good candidate for the DeNovo NT tissue implant.
18 - 55
Healthy Volunteers Needed
Duration of Participation
A period of five (5) years following the knee surgery.
Dennis C. Crawford, MD, PhD
Zimmer Orthobiologics, Inc.
Subjects will receive $50 for each post-operative visit required by the study, up to a maximum of $400 (total of eight (8) visits over the five (5) year duration of follow-up). Funds will be provided in the form of a Visa cash card.