A Prospective Randomized Study on Vanguard Cruciate Retaining Versus Vanguard High Flex Posterior Stabilized Total Knee System in the Early Range of Motion
Information source: Biomet, Inc.
Information obtained from ClinicalTrials.gov on November 03, 2008
Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Total Knee Arthroplasty
Intervention: Vanguard PS Knee (Device); Vanguard CR Knee (Device)
Phase: N/A
Status: Recruiting
Sponsored by: Biomet, Inc. Official(s) and/or principal investigator(s):
David Martin, MD, Principal Investigator, Affiliation: St. Catharines Hospital
Overall contact:
David Martin, MD, Phone: (905) 684-7271
Summary
Main Objectives are: Test Difference in terms of early ROM between Vanguard FB CR and
Vanguard FB PS. Knees; Demonstrate the comparable ROM of high flex PS to CR.
Clinical Details
Official title: A Prospective Randomized Study on Vanguard Cruciate Retaining Versus Vanguard High Flex Posterior Stabilized Total Knee System in the Early Range of Motion
Study design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Safety/Efficacy Study
Primary outcome: Knee Society Score
Secondary outcome: WOMACOxford Knee Complication
Eligibility
Minimum age: N/A.
Maximum age: N/A.
Gender(s): Both.
Criteria:
Patients need total knee replacement
Locations and Contacts
David Martin, MD, Phone: (905) 684-7271
St. Catharines Hospital, Ontario, Canada; Recruiting
David Martin, MD
Additional Information
Starting date: June 2007
Ending date: June 2011
Last updated: October 8, 2008
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