- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03130309
Results of a Mobile Unicompartimental Knee Prosthesis
Survival Rates of Atients Wearing a Mobile Unicompartimental Knee Prosthesis for the Past 10 Years
The unicompartmental knee prosthesis has become a routine procedure. Survival rate of over 90% after 10 years are generally reported. However, complications and reoperation may still occur for many reasons, and some of them may be related to component design: loosening (tibial above), polyethylene wear, knee stiffness, ligamentous instability, etc ... . Therefore, new designs can, at least in theory, improve the results of conventional models.
In this study, the investigators want to compare retrospectively data concerning survival rates of patients wearing unicompartmental knee prosthesis with mobile plate for over 10 years, with the ones published in the literature for conventional fixed-bearing prostheses and mobile-bearing prostheses
Study Overview
Status
Conditions
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Jean-Yves JENNY, MD, PhD
- Phone Number: 33.3.88.55.21.45
- Email: jean-yves.jenny@chru-strasbourg.fr
Study Locations
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Strasbourg, France, 67091
- Recruiting
- Centre de Chirurgie Orthopédique et de la Main (CCOM)
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Contact:
- Jean-Yves JENNY, MD, PhD
- Phone Number: 03 88 55 21 45
- Email: jean-yves.jenny@chrustrasbourg.fr
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients over 18 years
- Patients wearing unicompartmental knee prosthesis with mobile plate for over 10 years
Exclusion Criteria:
- Patients under 18 years
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Retrospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Compare retrospectively data concerning survival rates of patients wearingunicompartmental knee prosthesis with mobile plate for over 10 years, with the ones published in the literature for conventional fixed and mobile bearing prosthesis.
Time Frame: 10 years
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10 years
|
Collaborators and Investigators
Investigators
- Principal Investigator: Jean-Yves JENNY, MD, PhD, University Hospital, Strasbourg, France
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 6756
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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