Condition: Post Traumatic Arthritis · Osteoarthritis · Total Ankle Replacement · Sponsor: Stryker Trauma and Extremities
The goal of this study is to demonstrate the safety and performance of the Incompass™ Total Ankle System after surgery over the standard follow-up period. The study will measure improvements in patient-reported information related to quality of life and pain following surgery. In order to do this, medical imaging (i.e. X-Rays, CT scans) which have been taken as part of routine care, will be reviewed. Any additional X-Rays conducted during the period of the research will also be reviewed. The Incompass™ Total Ankle System has been cleared by the Food and Drug Administration (FDA). The products are already in use routinely in ankle replacement surgeries. No part of this study is experimental.
This description comes directly from the study's public registry record.
Caryn Thompson · 704-891-6540 · caryn.thompson@stryker.com
Rebecca Gibson · rebecca.gibson@stryker.com
Always discuss trial participation with your own doctor first.
| Illinois Bone and Joint Institute | Morton Grove, Illinois, United States | Recruiting |
| Baptist Health Louisville | Louisville, Kentucky, United States | Recruiting |
| Slocum Research & Education Foundation | Eugene, Oregon, United States | Recruiting |
| MUSC | Charleston, South Carolina, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07118501