DePuy Revision TKA Implant 5yr Survivorship

Clinical Outcome and 5-year Implant Survival Rate Among Adult Revision Total Knee Arthroplasty Patients With DePuy Implant Components

Status

Withdrawn

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01245478

Enrollment

Registered

2010-11-22

Start date

2010-11-30

Completion date

2012-07-31

Last updated

2013-05-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Complications; Arthroplasty, Mechanical

Keywords

Surgical Procedures, Elective

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.

Interventions

None listed

Study design

Observational model

CASE_ONLY

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

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

Outcome results