A Multicenter Study to Evaluate Functional Outcome After Knee Replacement
Stopped early · Not applicable
Conditions studied: Osteoarthritis
In brief
Patients will be consecutively enrolled by implant. Implant groups will be those who have undergone surgery with either a ConforMIS iTotal® CR TKA or an Off-the- Shelf (OTS) system. The patient will conduct functional testing and answer questionnaires. The results will compare the ConforMIS iTotal with an Off the Shelf Knee replacement.
Key facts
- Study ID
- NCT02494544
- Run by
- Restor3D
- People needed
- 215
- Starts
- 2015-07-01
- Expected to finish
- 2022-11-16
- Last updated by the study team
- 2025-11-21
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
Where it is running
- University of California in San Diego — La Jolla, California, United States
- Sharp Healthcare — San Diego, California, United States
- Denver-Vail Orthopedics — Parker, Colorado, United States
- Yale School of Medicine — New Haven, Connecticut, United States
- Tufts University — Boston, Massachusetts, United States
- University of Missouri — Columbia, Missouri, United States
- OrthoNY — Albany, New York, United States
- The Lindner Center for Research and Education — Cincinnati, Ohio, United States
Full record on ClinicalTrials.gov
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