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A Retrospective Study to Evaluate the ConforMIS iTotal® Posterior Stabilized (PS) Knee Replacement System

Osteo Arthritis Knee Clinical Trial

Official title:
A Retrospective Study to Evaluate the ConforMIS iTotal® Posterior Stabilized (PS) Knee Replacement System

Clinical Trial 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 ConforMIS iTotal PS knee product.

Clinical Trial 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 which have occurred since implantation as available. . All data will be collected from existing medical records and from single follow up call/email. - Demographics and Medical History - Pre & Post-Operative Data including Range of Motion - Surgical Data - Survivorship (phone/email or last known visit) - Patient Reported Outcomes (phone/email single time point visit) - Patient Satisfaction - KOOS Jr. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03289000
Study type Observational
Source Restor3D
Contact
Status Completed
Phase
Start date April 24, 2017
Completion date December 31, 2017
View Details
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