Study Results
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View full resultsBasic Information
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COMPLETED
186 participants
OBSERVATIONAL
2022-04-12
2023-06-27
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Study Groups
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VITAMIN E
Patients who received cemented total knee arthroplasty with vitamin E blended polyethylene mobile bearing
GKS Prime Flex Mobile knee
Total knee arthroplasty with a cemented mobile bearing bicompartmental knee prosthesis
POLYETHYLENE
Patients who received cemented total knee arthroplasty with conventional polyethylene mobile bearing
GKS Prime Flex Mobile knee
Total knee arthroplasty with a cemented mobile bearing bicompartmental knee prosthesis
Interventions
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GKS Prime Flex Mobile knee
Total knee arthroplasty with a cemented mobile bearing bicompartmental knee prosthesis
Eligibility Criteria
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Inclusion Criteria
* Minimum 7-year follow-up;
* Age ≥ 18 and \< 85 years;
* Patient who signed informed consent.
Exclusion Criteria
* Patient already enrolled in other clinical studies.
18 Years
85 Years
ALL
No
Sponsors
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Permedica spa
INDUSTRY
Responsible Party
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Principal Investigators
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Marco Spezia, MD
Role: PRINCIPAL_INVESTIGATOR
Ospedale Centro Ortopedico di Quadrante
Locations
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Ospedale Centro Ortopedico di Quadrante
Omegna, Verbania, Italy
Countries
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Provided Documents
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Document Type: Study Protocol and Statistical Analysis Plan
Other Identifiers
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VITALECOQ2020
Identifier Type: -
Identifier Source: org_study_id
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