Viewing Study NCT00160797



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Last Modification Date: 2024-10-26 @ 9:15 AM
Study NCT ID: NCT00160797
Status: WITHDRAWN
Last Update Posted: 2012-05-02
First Post: 2005-09-08

Brief Title: Total Knee Arthroplasty Outcome Study
Sponsor: University of Florida
Organization: University of Florida

Study Overview

Official Title: MIS Minimally Invasive Solutions Total Knee Arthroplasty Outcome Study 02-800
Status: WITHDRAWN
Status Verified Date: 2012-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: 102005 PI assigned duties as trauma physician in addition other duties
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief 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

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None