Observational Study of EVOLUTION® Revision CCK Knee Implants
This study is observing the long-term performance of specific knee implant components: the EVOLUTION® Revision Tibial System, EVOLUTION® Revision CCK Femur, and EVOLUTION® CCK Tibial Insert. These implants are used in revision knee arthroplasty (a surgery to replace a previous knee replacement). The main goal is to see how long these individual components last in patients over 10 years. You might be able to join if you are 21 or older, of any gender, and are having a revision knee surgery that uses these specific EVOLUTION® components. This is an observational study, meaning researchers will collect information about how the implants perform in real-world use. The study status is currently unclear.
- Study design
- This is an observational study, meaning researchers will collect information about the implants' performance without assigning treatments. It plans to enroll 45 participants.
- What's involved
- Not specified in the trial record.
- Compensation
- Not stated in the trial record.
- Follow-up
- Participants will be followed for 10 years after their surgery to assess how long the individual implant components last.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Post Market Clinical Follow-Up Study- EVOLUTION® Revision CCK
At a glance
Conditions
NCT04145401
Where you'd take part
This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
HCA Research Institute, OrthoONE at Swedish Medical Center
Englewood, Coloradono site contact published
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
What this trial measures
- Individual component survivorship10 years post-operative
Individual component survivorship for tibial base, femoral, and tibial insert at specified intervals out to 10 years follow-up.