Study to Evaluate Long Term Performance and Safety of the Knee Prosthesis (HLS KneeTec Deep Dish)
NCT ID: NCT05211141
Last Updated: 2024-07-16
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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TERMINATED
119 participants
OBSERVATIONAL
2017-02-28
2022-12-21
Brief Summary
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Detailed Description
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All patients treated with HLS KneeTec Deep Dish implant will be included. All eligible patients seen in consultation and who agree to participate in the study should be included, systematically and consecutively, since the initiation of the study.
Patients will be assessed according to the usual practice of the investigator at each participating site before surgery and then at the follow-up (FU) visits as following: 3 months (+/- 1 months); 15 months (+/- 3 months); 5 years (+/- 6 months) and 10 years (+/- 6 months).
Conditions
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Study Design
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COHORT
OTHER
Study Groups
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Patient with knee arthroplasty
patient with HLS KneeTec Deep Dish prosthesis
HLS KneeTec Deep Dish
total knee arthroplasty with HLS KneeTec Deep Dish prosthesis
Interventions
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HLS KneeTec Deep Dish
total knee arthroplasty with HLS KneeTec Deep Dish prosthesis
Eligibility Criteria
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Inclusion Criteria
* Implanted with an HLS KneeTec Deep Dish TKP according to the Instructions for Use (IFU) after the 1st of february, 2017
* Patients agree to consent to collect data from their medical records and agree to answer questionnaires for the purposes of the study.
Exclusion Criteria
18 Years
80 Years
ALL
No
Sponsors
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Corin
INDUSTRY
Responsible Party
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Principal Investigators
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Olivier ROCHE, MD
Role: PRINCIPAL_INVESTIGATOR
CHRU Nancy
Locations
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Chru de Nancy
Nancy, , France
Countries
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Other Identifiers
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CSP2017-07
Identifier Type: -
Identifier Source: org_study_id
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