ALknee Follow-up Study of the Cementless ATTUNE Rotating Platform and the Cementless LCS Rotating Platform Knee System

Study Results

Results pending

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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Recruitment Status

ACTIVE_NOT_RECRUITING

Total Enrollment

49 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-11-10

Study Completion Date

2029-05-31

Brief Summary

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The cementless ATTUNETM Rotating Platform Knee system was compared in a single-blind, randomized RSA trial to its predecessor, the LCS rotating platform Knee System. In this previous study, 61 knees were subjected to RSA examinations at 1-day and 3, 6, 12 and 24 months postoperative. This study found a promising equal migration of both tibial components and a lesser migration of the femoral component of the ATTUNETM knee system after two years, although with a similar migration rate between year 1 and 2. this raises the question of whether the migration of the prostheses relative to each other will increase or remain the same in the long term. To examine this, a mid-and long-term RSA follow-up to measure migration is necessary. In addition, another new RSA measurement parameter has become known in recent years that may provide an indication of the bonding of the prosthesis to the bone at the time of measurement. This new parameter, called the Induced Displacement (ID) of a prosthesis, measures the position and orientation relative to the bone while the prosthesis is under different loading conditions (e.g., patient in supine or standing position). This means that a large measured difference between these different loading condition measurements would indicate that osseointegration of the prosthesis never occurred or is no longer present. To improve the understanding of the tendency of both prostheses to aseptic loosening after a mid- to long-term follow up, migration over time and inducible displacement analyses are necessary.

The primary objective of this study is to accurately compare mid- and long-term migration of two uncemented TKR prostheses. The secondary objectives of this study are to evaluate if inducible displacement can be used as a parameter to detect loose implants, and to compare inducible displacement, clinical and radiological outcome and patient-reported outcomes (PROMS) after a follow-up of 5 and 10 years of two uncemented TKR prostheses.

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Detailed Description

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Conditions

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Total Knee Arthroplasty Total Knee Replacement Knee Osteoarthritis

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Cementless ATTUNE

Cementless ATTUNE Rotating Platform Cruciate Sacrificing Knee System

Radiographs of the knee for radiostereometric analysis (RSA)

Intervention Type RADIATION

RSA radiographs will be made 5 and 10 years after the total knee arthroplasty.

Cementless LCS

Cementless LCS rotating platform Cruciate Sacrificing Knee System

Radiographs of the knee for radiostereometric analysis (RSA)

Intervention Type RADIATION

RSA radiographs will be made 5 and 10 years after the total knee arthroplasty.

Interventions

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Radiographs of the knee for radiostereometric analysis (RSA)

RSA radiographs will be made 5 and 10 years after the total knee arthroplasty.

Intervention Type RADIATION

Eligibility Criteria

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Inclusion Criteria

In order to be eligible to participate in this study, a subject must meet all of the following criteria:

* The Patient participated in the initial study (NL58911.058.16) \[1\].
* The patient is capable of giving informed consent and expressing a willingness to comply with the study.

Exclusion Criteria

A potential subject who meets any of the following criteria will be excluded from participation in this study:

* The patient underwent a major revision TKR (exchange of the tibial or femoral component).
* The patient is unable or unwilling to sign the informed consent specific to this study.

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes