C3 Total Joint Patient Registry

This registry will prospectively collect a core set of data on patients undergoing knee or
hip replacement. This registry will include a variety of different products, implants,
technologies and procedures. The registry will also collect any adverse events/complications
that occur during or following these surgeries. This database can also be utilized in the
future to answer research questions, by retrospectively going back through the data. This
information also may go to insurance companies or hospitals for quality measurement and
metrics reporting. The data will be utilized to develop strategic treatment pathways that
will improve patient care. Ultimately, the goal of the registry is to enhance the
understanding of treatment associated with knee and hip replacement and the resulting
patient outcomes. The registry will also be used to provide quality measurement and metrics
reporting.

Inclusion Criteria:

- At least 18 years of age

- Undergoing knee or hip replacement

- Subject is likely to follow standard of care post-operative follow up for at least 1
year

Exclusion Criteria:

- Inability to complete follow-up visits or required questionnaires

- Inability to provide informed consent without a legally authorized representative