A Prospective, Multicenter Study to Evaluate the ConforMIS iTotal® (CR) Knee Replacement System
NCT01820650 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 359
Last updated 2023-10-25
Summary
This study is designed to observe the long term clinical outcomes of patient-specific knee arthroplasty in patients with osteoarthritis.
Conditions
- Osteoarthritis of the Knee
Interventions
- DEVICE
-
iTotal G2 CR Knee Replacement System
Total Knee replacement
Sponsors & Collaborators
-
Restor3D
lead INDUSTRY
Principal Investigators
-
Marc Quartulli · Restor3D
-
Terry Clyburn, MD · The University of Texas Health Science Center, Houston
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2013-02-28
- Primary Completion
- 2017-03-31
- Completion
- 2023-10-31
- FDA Device
- Yes
Countries
- United States
Study Locations
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