NCT01500252View on ClinicalTrials.gov

Patellar Resurfacing Versus Patellar Retention in Total Knee Arthroplasty - A Randomized Clinical Trial

PHASE4CompletedINTERVENTIONAL
Enrollment

38

Participants

Timeline

Start Date

September 30, 1996

Primary Completion Date

June 30, 2004

Study Completion Date

December 31, 2009

Conditions
Total Knee Replacement
Interventions
DEVICE

Patellar Replacement Prosthesis

The Profix™ Total Knee System, a posterior cruciate retaining prosthesis manufactured by Smith and Nephew, Inc. was utilized in all subjects. Subjects randomized to the Resurfaced group received an all polyethylene patellar implant

DEVICE

Profix TKR with Patellar Retention

All subjects received a Profix TKR. Subjects in the Patellar Retention group retained their native patellar surface.

Trial Locations (1)

T6G 2B7

University of Alberta Hospital, Edmonton

All Listed Sponsors
collaborator

Smith & Nephew, Inc.

INDUSTRY

lead

University of Alberta

OTHER

NCT01500252 - Patellar Resurfacing Versus Patellar Retention in Total Knee Arthroplasty - A Randomized Clinical Trial | Biotech Hunter | Biotech Hunter