Post Market Clinical Follow Up of LEGION™ Primary TKS With VERILAST™

NCT ID: NCT02380092

Last Updated: 2025-12-15

Basic Information

• Recruitment Status: ACTIVE_NOT_RECRUITING
• Total Enrollment: 163 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2015-09-30
• Study Completion Date: 2029-05-31

Brief Summary

LEGION™ Primary Total Knee System is CE-marked and marketed in all study regions. This study serves as post-market surveillance for LEGION™ Primary Total Knee System with the VERILAST™ bearing surface (OXINIUM™ femoral component with highly cross-linked polyethylene tibial insert).

All study subjects will receive a LEGION™ Primary Total Knee System with VERILAST™ bearing surface and the results will be analysed against historical data from patients who received a Genesis II knee replacement.

Detailed Description

The LEGION™ Primary Total Knee System (TKS) is a comprehensive, state-of-the-art system that empowers surgeons to address diverse surgical challenges and provide personalized joint care. The LEGION™ Primary TKS implant designs were built on the legacy of the GENESIS™ II TKS. For more than 15 years and in more than 30 countries, the GENESIS™ II TKS has achieved outstanding clinical outcomes.

As CE-mark and 510k approval for the LEGION™ Primary TKS has been obtained, it is being used in clinical practice in several countries including Europe and the US but clinical studies need to be carried out in order to confirm its safety and efficacy and in order to conform to the medical device directives (MEDDEV. 2.7.1 Rev.3).

This study is therefore a post-market study to evaluate the short-, mid- and long-term safety and effectiveness of the LEGION™ Primary TKS with VERILAST™ bearing surface (the combination of an OXINIUM™ femoral component with highly cross-linked polyethylene tibial base plate inserts). The clinical outcome from a large cohort of subjects who are treated with the LEGION™ Primary TKS as part of their standard of care will be documented. The study is designed to reflect standard clinical practice as closely as possible because it allows the results of such a study to represent the true clinical outcome that would be achieved in clinical practice, up to a maximum. Only subjects who will be treated with the LEGION™ Primary TKS as part of their normally planned care will screened for participation in this study.

Conditions

Degenerative Joint Disease

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Interventions

LEGION™ Primary TKS with VERILAST™ Bearing Surface

All study subjects will be treated with LEGION™ Primary TKS with VERILAST™ Bearing Surface as per standard clinical practice.

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• Subject requires primary TKA and has elected to use the LEGION™ Primary TKS with VERILAST™.
• Subject requires primary TKA due to degenerative joint disease (primary osteoarthritis, post-traumatic arthritis, avascular necrosis, rheumatoid arthritis).
• Subject is of legal age to consent, agrees to consent to and to follow the study visit schedule (as defined in the study protocol and informed consent form), by signing the EC approved informed consent form.
• Routine radiographic assessment is possible.
• Subject plans to be available through ten (10) years postoperative follow-up.
• Subject is 18-75 years of age at the time of surgery.

Exclusion Criteria

• Age > 75 years at the time of surgery.
• Subjects with immunosuppressive disorders.
• Subject has severe pronation of the ipsilateral foot or any other relevant clinical condition contributing to abnormal ambulation (including but not limited to ankle fusion, ankle arthroplasty, previous hip fracture, ipsilateral hip arthritis resulting in flexion contracture).
• Subject has undergone a previous major surgery to the study knee (including osteotomy, fracture fix, medial or lateral ligament surgery).
• Subject has active infection or sepsis (treated or untreated).
• At the time of enrollment, subject has one or more of the following arthroplasties that are not fully healed and well-functioning, as determined by the Investigator:

• Ipsilateral or contralateral primary total hip arthroplasty or hip resurfacing arthroplasty.
• Contralateral primary total knee or unicondylar knee arthroplasty.
• Subject has presence of malignant tumor, metastatic, or neoplastic disease.
• Subject has conditions that may interfere with the TKA survival or outcome (i.e., Paget's or Charcot's disease, muscular atrophy, uncontrolled diabetes, moderate to severe renal insufficiency or neuromuscular disease).
• Subject has any acute or chronic morbidity of vascular origin that, in the opinion of the Investigator, is likely to compromise successful treatment or compliance to follow-up visits.
• Subject has inadequate bone stock to support the device (severe osteopenia, family history of severe osteoporosis or osteopenia).
• Subject has an emotional or neurological condition that would pre-empt their ability or willingness to participate in the study.
• Subject has a Body Mass Index (BMI) >40.0.
• Subject requires revision TKA.
• Subject is expected to require bilateral TKA within 1 year following study knee replacement.
• Subject does not understand the language used in the Informed Consent Form.
• Subject is enrolled in another clinical study at the same time.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Smith & Nephew, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Karlie Morgan

Role: STUDY_DIRECTOR

Director of Clinical Study Management, Global Clinical Research Operations

Locations

Evangelisches Krankenhaus Wien

Vienna, , Austria

Orthopadische Krankenhaus Gersthof

Vienna, , Austria

AMEOS Klinikum Seepark Geestland

Langen, Kreis Geestland, Germany

OrthoCentrum

Hamburg, , Germany

CaritasKlinikum St. Joseph Saarbrücken-Dudweiler

Saarbrücken-Dudweiler, , Germany

KniePraxis Prof. Dr. Tibesku

Straubing, , Germany

Servicio de C.O.T. Hospital Clínico Universitario de Santiago de Compostela

Santiago de Compostela, , Spain

Countries

Austria; Germany; Spain

Other Identifiers

12-4042-01

Identifier Type: -

Identifier Source: org_study_id