Study of the ConforMIS iDuo(R) G2
NCT01564641 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 150
Last updated 2023-10-25
Summary
To evaluate the ConforMIS iDuo G2 implant
Conditions
- Bicompartmental Osteoarthritis
Interventions
- DEVICE
-
iDuo G2
single comparator
Sponsors & Collaborators
-
Restor3D
lead INDUSTRY
Principal Investigators
-
L Rolston, MD · Forest Ridge
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2012-05-31
- Primary Completion
- 2016-08-31
- Completion
- 2022-11-18
- FDA Device
- Yes
Countries
- United States
Study Locations
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