DePuy Revision TKA Implant 5yr Survivorship
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|ClinicalTrials.gov Identifier: NCT01245478|
Recruitment Status : Withdrawn (Retrospective record review only (no subject enrollment). Contract never executed between Sponsor and Site.)
First Posted : November 22, 2010
Last Update Posted : May 1, 2013
This will be a retrospective chart review of 200 charts of adult patients who have undergone a revision TKA at New England Baptist Hospital and who received implant component(s) manufactured by DePuy Orthopedics. The data will be collected retrospectively after patients are seen clinically for a minimum of five years after surgery to answer:
- What is the five-year survivorship of revision a knee prosthesis containing components manufactured by DePuy Orthopedics among adult revision TKA patients?
- What patient factors are associated with the need for re-operation after revision TKA among patients receiving DePuy implant components? How do clinical outcomes change from baseline over the five-year follow-up after revision TKA surgery?
Data collection will include patient-reported and clinician-reported measures.
|Condition or disease|
|Complications; Arthroplasty, Mechanical|
|Study Type :||Observational|
|Actual Enrollment :||0 participants|
|Official Title:||Clinical Outcome and 5-year Implant Survival Rate Among Adult Revision Total Knee Arthroplasty Patients With DePuy Implant Components|
|Study Start Date :||November 2010|
|Actual Primary Completion Date :||July 2012|
|Actual Study Completion Date :||July 2012|
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01245478
|Principal Investigator:||John Richmond, MD||New England Baptist Hospital|