Total Joint Revisions
Conditions
Brief summary
The goal of this is to improve durability of total joint replacements in patients, thereby improving clinical outcomes and implant performance. To reach this objective, our research program would like to assess the safety, efficacy, performance, and durability of FDA approved biomaterial and implant designs used in joint replacements.
Detailed description
The objective of the investigation will be to determine the mechanism of material failure and identify any design features that put the implant at risk for early failure. Normally all implants are discarded. The investigators will collect the implants indicated for removal and if there are impressive findings the investigators will perform research on the implants, otherwise the implants will be discarded. All patients will be followed prospectively after informed consent is signed. The implants that are chosen for research will be assessed for implant wear and failure at a lab appropriate for evaluating the particular concern.
Interventions
None listed
Sponsors
University of Utah
Study design
Observational model
CASE_ONLY
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
Yes
Inclusion criteria
* Patients who will be undergoing revision total joint surgery will be asked to participate in this study.
Exclusion criteria
* Patients who are not undergoing revision total joint surgery.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| determine the mechanism of material failure | 10 years |
Secondary
| Measure | Time frame |
|---|---|
| identify any design features that put the implant at risk for early failure. | 10 years |
Countries
United States
Outcome results
None listed