Total Knee Arthroplasty Outcome Study

Total Knee Replacement Clinical Trial

Official title:

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

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT00160797
• Other study ID #: 580-2004
• Status: Withdrawn
• Phase: Phase 4
• First received: September 8, 2005
• Last updated: April 30, 2012
• Start date: August 2005
• Est. completion date: October 2005

Study information

• Verified date: April 2012
• Source: University of Florida
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

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

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.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: October 2005
• Est. primary completion date: October 2005
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Presence of a severely disabled joint secondary to painful osteoarthritis, rheumatoid arthritis, or post-traumatic arthritis that warrants primary knee arthroplasty.

• Gender - Males and females will be included. The male-to-female ratio will depend upon the patient population at each institution conducting the study.

• Age - Minimum of 18 years-old.

• Stable Health - The patient should be able to undergo surgery and participate in a follow-up program based upon physical examination and medical history.

• Patient or patient's legal representative has read and signed the Letter to the Patient form.

Exclusion Criteria:

• Patient is skeletally immature.

• Previous ipsilateral knee arthroplasty.

• Previous Patellectomy.

• Patient is pregnant or breastfeeding.

• Presence of clinically significant disease of the cardiovascular, renal, hepatic, hematologic, respiratory, endocrine, neurological, gastrointestinal, genitourinary, immune systems or other medical condition which is not well controlled.

• Patients who have received an investigational drug or device within the last 30 days.

• Patient is unwilling or unable to cooperate in a follow-up program.

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

Intervention

Device:
• MIS™ Minimally Invasive Solutions™ TKA System

Locations

Country	Name	City	State
n/a

Sponsors (2)

Lead Sponsor	Collaborator
University of Florida	Zimmer, Inc.