DePuy Revision TKA Implant 5yr Survivorship

Withdrawn

• Conditions: Complications; Arthroplasty, Mechanical

• Registration Number: NCT01245478
• Lead Sponsor: The New England Baptist Hospital

Brief Summary

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.

Detailed Description

Not available

Study Timeline

• Study Start: 2010-11
• Study First Submitted: 2010-11-19
• Study First Submitted QC: 2010-11-19
• Study First Posted: 2010-11-22
• Primary Completion: 2012-07
• Study Completion: 2012-07
• Status Verified: 2013-04
• Last Update Submitted: 2013-04-30
• Last Update Posted: 2013-05-01

Recruitment & Eligibility

• Status: WITHDRAWN
• Sex: All
• Target Recruitment: Not specified

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

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified