A Prospective Randomized Study on Vanguard Cruciate Retaining Versus Vanguard High Flex Posterior Stabilized Total Knee System in the Early Range of Motion
NCT ID: NCT00763113
Last Updated: 2017-06-16
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
173 participants
INTERVENTIONAL
2007-06-30
2012-07-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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1
Vanguard PS Knee
Vanguard PS Knee
Vanguard PS Knee
2
Vanguard CR Knee
Vanguard CR Knee
Vanguard CR Knee
Interventions
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Vanguard PS Knee
Vanguard PS Knee
Vanguard CR Knee
Vanguard CR Knee
Eligibility Criteria
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Inclusion Criteria
ALL
No
Sponsors
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Zimmer Biomet
INDUSTRY
Responsible Party
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Principal Investigators
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David Martin, MD
Role: PRINCIPAL_INVESTIGATOR
St. Catharines Hospital
Locations
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St. Catharines Hospital
Ontario, , Canada
Countries
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Other Identifiers
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BMET CA 01
Identifier Type: -
Identifier Source: org_study_id
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