NCT02178020View on ClinicalTrials.gov

Outcome Study of Highly-cross Linked Polyethylene vs. Standard Polyethylene for Primary Posterior Stabilized (PS) Total Knee

UnknownOBSERVATIONAL
Enrollment

500

Participants

Timeline

Start Date

July 31, 2009

Primary Completion Date

July 31, 2019

Study Completion Date

July 31, 2019

Conditions
Arthroplasty, Replacement, Knee
Interventions
DEVICE

knee arthroplasty, standard polyethylene

total knee replacement follow-up; clinical and radiographic; revision rate

DEVICE

knee arthroplasty, XLP polyethylene

total knee arthroplasty with highly crosslinked polyethylene tibial liner

Trial Locations (1)

27514

Chapel Hill Orthopedic Surgery and Sports Medicine, Chapel Hill

Sponsors

Collaborators (1)

Zimmer Biomet
All Listed Sponsors
collaborator

Zimmer Biomet

INDUSTRY

lead

Chapel Hill Orthopedics Surgery & Sports Medicine

OTHER

NCT02178020 - Outcome Study of Highly-cross Linked Polyethylene vs. Standard Polyethylene for Primary Posterior Stabilized (PS) Total Knee | Biotech Hunter | Biotech Hunter