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Clinical Trial Summary

The primary purpose of this investigation is to report the short-term clinical outcomes (2-3 years) of patellofemoral arthroplasty implanted using the MAKOplasty knee resurfacing system.


Clinical Trial Description

The primary purpose of this investigation is to report the short-term clinical outcomes of patellofemoral arthroplasty implanted using the MAKOplasty knee resurfacing system.

The secondary purpose is to compare the short-term outcomes, complication rates, and survival rates of this operation to those of our historical controls of patients who underwent either osteochondral autograft transfer or autologous chondrocyte implantation for full-thickness patellofemoral articular cartilage lesions. The investigators believe these data will provide strong evidence to improve the selection criteria for patellofemoral arthroplasty.

All patients will complete validated questionnaires from the Cincinnati Knee Rating System, including the Sports Activity and Function Form, the Occupational Rating Form, and the Symptom Rating Form. Patients will also complete the SF-12 general health questionnaire. In addition to the above mentioned rating systems, patients will also complete questionnaires on post-surgical expectations and general fitness level. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02738476
Study type Observational [Patient Registry]
Source Cincinnati Sportsmedicine Research and Education Foundation
Contact Frank R Noyes, MD
Phone 513-347-9999
Email frnoyes@gmaili.com
Status Recruiting
Phase
Start date April 2016
Completion date February 2022

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