NCT00160797

Total Knee Arthroplasty Outcome Study

MIS™ Minimally Invasive Solutions™ Total Knee Arthroplasty Outcome Study #02-800

• Status: Withdrawn
• Phase: Phase 4
• Study type: Interventional
• Enrollment: 0 (actual)
• Sponsor: University of Florida · Academic / Other
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

The purpose of this study is to gather information about total knee replacement surgery using minimally invasive surgical procedures.

Detailed description

The purpose of this study is to gather information about total knee replacement surgery using minimally invasive surgical procedures. The MIS™ Minimally Invasive Solutions™ Total Knee Arthroplasty System has been cleared for use by the Food and Drug Administration. You are invited to participate in this data collection study, comparing the MIS system to standard knee replacement systems. The decision about which system and operation will be best for you has already been made by you and your orthopaedic surgeon. The information will be used to compare minimally invasive surgery and the standard surgery procedures. The results of this study will provide information that will add to the knowledge base of knee replacement surgery.

Conditions

• Total Knee Replacement

Interventions

Type	Name	Description
DEVICE	MIS™ Minimally Invasive Solutions™ TKA System

Timeline

• Start date: 2005-08-01
• Primary completion: 2005-10-01
• Completion: 2005-10-01
• First posted: 2005-09-12
• Last updated: 2012-05-02