Total Knee Arthroplasty Outcome Study

Status Withdrawn

Clinical Trial Summary

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

Clinical Trial 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. ;

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Total Knee Replacement

Clinical Trial Details

NCT number	NCT00160797
Study type	Interventional
Source	University of Florida
Contact
Status	Withdrawn
Phase	Phase 4
Start date	August 2005
Completion date	October 2005

View Details

See also
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