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Clinical Trials/NCT03568123
NCT03568123CompletedNot Applicable

A Prospective Randomized Control Study on CR vs MC Polyethylene Bearing With Persona Total Knee System in Total Knee Arthroplasty

Anders Troelsen1 site in 1 country60 target enrollmentStarted: July 5, 2017Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
60
Locations
1
Primary Endpoint
Radiostereometric analysis (RSA)

Study Overview

Brief Summary

Knee replacement is an established treatment for late stage osteoarthritis (OA) of the knee (Charnley et al. 1961). Recently, Zimmer-Biomet have introduced Persona Total Knee system with design changes that include asymmetric tibia plate, increased medial pivoting and more extensive choices in respect to poly thickness, all with the purpose to improve balancing, stability and longevity. One design change that is introduced is the medial congruent (MC) polyethylene to be used instead of standard cruciate retaining (CR) design. The theoretic proposed benefit of MC polyethylene bearing is improved kinematics mimicking native knee motion. However, currently no studies exist evaluating outcome following use of MC polyethylene bearing. Therefore such design changes and proposed benefits need to be evaluated in a prospective clinical trail, with focus on patient safety, satisfaction and implant durability.

In this project the investigators wish to:

Evaluate stability and fixation, intra-operative and postop complications, survivorship and patient reported outcome measures following primary total knee replacement using MC polyethylene bearing compared to CR polyethylene bearing with Persona Total Knee for treatment of knee osteoarthritis.

This project is carried out as a 2-arm randomized controlled single-blinded trial, in which the clinical and radiological outcomes after treatment of knee osteoarthritis with insertion of either 1) Persona Total Knee System with MC polyethylene bearing or 2) Persona Total Knee System with CR polyethylene bearing are compared. Recruitment of participants to this project is expected to begin in October 2016 or as soon as permission from the Regional Ethics Committee and the Danish Data Protections Agency is obtained. A total of 60 participants are to be included at Hvidovre University Hospital. Recruitment is expected completed after a period of 1.5 year. The project is expected to be completed 2 years after recruitment of the last participant (2019).

Participants are seen on an outpatient basis at 3 months, 1 and 2 years postoperatively. RSA is performed postoperatively and at all outpatient follow-ups. Dynamic RSA is performed at 1 year follow-up. The patients will be followed for survival through The Danish Knee Arthroplasty Registry.

This project is financed by Zimmer-Biomet®, Warsaw, Indiana, USA. The primary investigator of this project has independently initiated the project.

Detailed Description

Background Knee replacement is an established treatment for late stage osteoarthritis (OA) of the knee (Charnley et al. 1961). There are different approaches to prosthetic replacement and current practices and designs are often based on limited evidence (Plate et al. 2012). There have been individual cohort studies, indirect comparisons and retrospective studies to test the efficacy of a variety of different total knee replacement devices but there are very few high quality investigations of new paradigms or significant design change. Those studies that do exist have usually been undertaken to address a combination of design changes and many involve only short-term assessments (Mäkelä et al. 2008). Ongoing research and development programs for knee replacement are increasingly taking account of the needs of the changing characteristics of the late stage OA knee population.

There is an increasing demand for joint replacement in a younger population (Mäkelä et al. 2014). Due to the changing demographics of joint replacement, the population of younger patients are seeking options that not only correct their disease or deformity, but do not limit them in activity (Geerdink et al. 2009). Activities of daily living take higher priority in this patient group, and patients needing total joint replacement do not have many options that accommodate higher levels of activity.

Studies have shown that modern implant designs can potentially improve outcome. Therefore new implants are introduced to the marked with the theoretical benefit of improved implant survival and superior patient reported outcomes. Within Total knee arthroplasty, design changes are introduced in attempt to improve knee kinematics, improve alignment and functionality, but those potential improvements need to be evaluated Recently, Zimmer-Biomet have introduced Persona Total Knee system with design changes that include asymmetric tibia plate, increased medial pivoting and more extensive choices in respect to poly thickness, all with the purpose to improve balancing, stability and longevity. One design change that is introduced is the medial congruent (MC) polyethylene to be used instead of standard cruciate retaining (CR) design. The theoretic proposed benefit of MC polyethylene bearing is improved kinematics mimicking native knee motion. However, currently no studies exist evaluating outcome following use of MC polyethylene bearing. Therefore such design changes and proposed benefits need to be evaluated in a prospective clinical trail, with focus on patient safety, satisfaction and implant durability.

The purpose of the proposed Randomized Clinical Trial (RCT) is to evaluate the outcome and safety of a newly designed polyethylene bearing by comparing it with a control group of patients implanted with an established polyethylene bearing.

Device description

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Outcomes Assessor)

Masking Description

Participants are unaware of which prosthesis they receive and the research coordinator handling the collected questionnaires postoperatively is also unaware of which prosthesis the participant has received. The research assistant handling both standard RSA as well as dynamic RSA analysis is also unaware of which prosthesis the participant has received

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Clinical and radiological osteoarthritis of the knee set to receive a primary unilateral total knee replacement
  • •>18 years of age
  • •Participants must be able to speak and understand Danish
  • •Participants must be able to give informed consent and be cognitively intact
  • •Participants must be able to complete all post-operative controls
  • •Participants must not have severe comorbidities, American Society of Anesthesiologists Physical Status Classification System (ASA) score ≤ 3
  • •Clinically suitable to receive a Cruciate Retaining (CR) implant (no severe deformity and/or ligament instability)

Exclusion Criteria

  • •Age under 18 years.
  • •Terminal illness
  • •Revision knee replacement surgery
  • •Rheumatoid Arthritis
  • •Traumatic etiology
  • •Prior surgery on the affected knee that includes osteosynthesis, anterior cruciate ligament (ACL) and/or posterior cruciate ligament (PCL) and/or collateral ligament surgery. Arthroscopy with meniscectomy / cartilage surgery / house cleaning is allowed.
  • •Altered pain perception and / or neurologic affection due to diabetes or other disorders.
  • •Patients will be excluded intraoperative if CR implant is not suitable.

Arms & Interventions

MC polyethylene bearing

Experimental

Persona Total Knee System with MC polyethylene bearing

Intervention: MC polyethylene bearing (Device)

CR polyethylene bearing

Active Comparator

Persona Total Knee System with a CR polyethylene liner.

Intervention: CR polyethylene bearing (Device)

Outcomes

Primary Outcomes

Radiostereometric analysis (RSA)

Time Frame: 2 years after postoperatively

Radiologically verified stability and fixation is measured as the Maximum total point motion (MTPM) using RSA

Secondary Outcomes

  • Radiostereometric analysis (RSA)(1 year postoperatively)
  • Oxford Knee Score - Activity & Participation Questionnaire (OKS-APQ)(Change from preoperative to 2 years postoperatively)
  • Oxford Knee Score (OKS)(Change from preoperative to 2 years postoperative OKS)
  • EuroQol 5-dimension (EQ-5D)(Change from preoperative to 2 years postoperatively)
  • Forgotten Joint Score (FJS)(Change from preoperative to 2 year postoperatively)
  • Adverse Events(Through study completion, up to 2 years postoperatively)
  • Radiolucency / osteolysis(immediate postoperatively and 1 and 2 years postoperatively)
  • Dynamic RSA(1 year postoperatively)
  • Radiostereometric analysis (RSA)(3 months postoperatively)
  • Oxford Knee Score (OKS)(Change from preoperative to 3 months postoperative OKS)
  • Oxford Knee Score (OKS)(Change from preoperative to 1 year postoperative OKS)
  • Oxford Knee Score - Activity & Participation Questionnaire (OKS-APQ)(Change from preoperative to 3 months postoperatively)
  • Oxford Knee Score - Activity & Participation Questionnaire (OKS-APQ)(Change from preoperative to 1 year postoperatively)
  • EuroQol 5-dimension (EQ-5D)(Change from preoperative to 3 months postoperatively)
  • EuroQol 5-dimension (EQ-5D)(Change from preoperative to 1 year postoperatively)
  • Forgotten Joint Score (FJS)(Change from preoperative to 3 months postoperatively)
  • Forgotten Joint Score (FJS)(Change from preoperative to 1 year postoperatively)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Anders Troelsen

Professor

Hvidovre University Hospital

Study Sites (1)

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