NCT00755144

A Randomized Control Trial to Assess Early Clinical and Functional Outcome of the ROCC and LCS Total Knee Implant Designs

A Prospective Randomized Study on Early Clinical and Functional Outcome of the ROCC and LCS Total Knee Arthroplasty Implant Designs

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 200 (actual)
• Sponsor: Zimmer Biomet · Industry
• Sex: All
• Age: 80 Years
• Healthy volunteers: Not accepted

Summary

This is a prospective Randomised Control Trial to compare the Early Clinical and Functional Outcome of the ROCC and LCS total knee arthroplasty implant designs.

Detailed description

This study compares two similar designs of cementless rotating bearing total condylar knee replacements. The study will be conducted at a single clinical unit with a senior orthopaedic surgeon implanting all devices.Their performances will be assessed by clinical scores and comprehensive function outcome documentation undertaken by qualified physiotherapists. The persons undertaking the assessments will be blinded to which implants the patients have.

Conditions

• Osteoarthritis

Interventions

Type	Name	Description
DEVICE	LCS Knee	Cementless total knee arthroplasty with LCS Knee
DEVICE	ROCC Knee	Cementless total knee arthroplasty with ROCC Knee

Timeline

• Start date: 2007-04-01
• Primary completion: 2011-01-01
• Completion: 2011-01-01
• First posted: 2008-09-18
• Last updated: 2017-06-20

Locations

1 site across 1 country: United Kingdom