DePuy Revision TKA Implant 5yr Survivorship

The New England Baptist Hospital

Status: Withdrawn

Conditions: Complications; Arthroplasty, Mechanical

Study type: Observational

Funder types: Other; Industry

Identifiers

NCT01245478

IIS-000105

Details and patient eligibility

About

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:

1. What is the five-year survivorship of revision a knee prosthesis containing components manufactured by DePuy Orthopedics among adult revision TKA patients?
2. 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.

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Received a Revision TKA (must have been initial revision)

  --Received J&J/DePuy implant components for initial revision

• Procedure performed at New England Baptist Hospital

Exclusion criteria

• 2nd Revision TKA on knee
• Received femoral or tibial components not of DePuy manufacture