Status:
COMPLETED
A Retrospective Study to Evaluate the ConforMIS iTotal® Posterior Stabilized (PS) Knee Replacement System
Lead Sponsor:
Restor3D
Conditions:
Osteo Arthritis Knee
Eligibility:
All Genders
18+ years
Brief Summary
This study is a retrospective, multi-center study, with one single remote follow up contact. This study will include a minimum of 80 patients and a maximum 100 patients who have been treated with the ...
Detailed Description
Patients will be contacted either by phone or email for a single remote follow-up. Retrospective data will be collected from medical records including pre-operative, operative and any follow up visits...
Eligibility Criteria
Inclusion
- Previously underwent surgical implantation of a ConforMIS iTotal PS knee replacement.
- Over 18 Years of age
Exclusion
- 1\. BMI \> 40
Key Trial Info
Start Date :
April 24 2017
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
December 31 2017
Estimated Enrollment :
93 Patients enrolled
Trial Details
Trial ID
NCT03289000
Start Date
April 24 2017
End Date
December 31 2017
Last Update
October 25 2023
Active Locations (2)
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1
Tennessee Orthopaedic Alliance
Nashville, Tennessee, United States, 37203
2
Scott Orthopedic Center
Huntington, West Virginia, United States, 25702