A Prospective Study to Evaluate the ConforMIS iTotal® (PS) Knee Replacement System
NCT03152162 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 102
Last updated 2023-10-25
Summary
This is a prospective clinical study designed to observe the long-term clinical outcomes of total knee arthroplasty using a patient-specific, posterior stabilized implant in patients with osteoarthritis.
Conditions
- Osteoarthritis, Knee
Interventions
- DEVICE
-
iTotal PS KRS
Total knee arthroplasty for treatment of osteoarthritis
Sponsors & Collaborators
-
Restor3D
lead INDUSTRY
Principal Investigators
-
Marc Quartulli · Restor3D
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2017-05-01
- Primary Completion
- 2022-11-01
- Completion
- 2022-11-01
- FDA Device
- Yes
Countries
- United States
Study Locations
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