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OpenTrials
Completed

NCT Number: NCT00763113

A Prospective Randomized Study on Vanguard Cruciate Retaining Versus Vanguard High Flex Posterior Stabilized Total Knee System in the Early Range of Motion

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.

Completed

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Key information

Conditions

Total Knee Arthroplasty

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

St. Catharines Hospital

Ontario, Canada

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Patients need total knee replacement

Treatment and study plan

Vanguard PS Knee

Device

Vanguard PS Knee

Vanguard CR Knee

Device

Vanguard CR Knee

Primary outcomes

  1. Knee Society Score

    Time frame: 6weeks, 6months, 1 year

Secondary outcomes

  1. WOMAC

    Time frame: 6weeks, 6months, 1 year

  2. Oxford Knee

    Time frame: 6weeks, 6months, 1 year

  3. Complication

    Time frame: Anytime

Sponsors and collaborators

Lead sponsor

Zimmer Biomet

Industry

Registry information

Important dates

Study start
2007
Primary completion
2012
Study completion
2012
First posted
Sep 30, 2008
Registry last updated
Jun 16, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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