Skip to main content
OpenTrials
Active, Not Recruiting

NCT Number: NCT02798432

Hybrid Versus Cemented TKA Using the NexGen LPS Prosthesis

Early total knee arthroplasty (TKA) implant systems most frequently used an all-polyethylene cemented tibial component1. Based on finite-element analysis studies reporting superior force distribution compared with conventional all-polyethylene components, metal-backed tibial baseplates have dominated the TKA implant market since the middle of the 1980's2. These modular implants provided excellent long-term implant survivorship3.

As TKA became increasingly successful, younger patients increasingly became eligible. Increasing life expectancy has raised the concern that cemented TKAs may not withstand prolonged use, particularly in younger patients4. Patients younger than 65 years are projected to account for more than 50% of patients undergoing TKA by 2016 and to more than 50% of patients undergoing revision surgery by 2011. The number of total knee revisions in the United States is expected to increase from 38,300 in 2005 to 268,200 in 20305.

Many authors have reported excellent and equivalent results of cemented and cementless TKA6-8. Despite these encouraging reports, the major concern with cementless TKA has been the tibial component, and, therefore, the preference for many surgeons still remains to cement the tibial component9,10. The femoral component may be the most suitable for cementless fixation11-13. However, the best femoral method of fixation is still being discussed. Currently, the decision to cement or not to cement the femoral component is based on the surgeon's preference14.

The current study was designed to compare the hybrid NexGen LPS (Zimmer Inc, Warsaw, IN) and the cemented NexGen LPS. The purpose of this study is to establish whether the hybrid NexGen LPS leads to equally successful results as the cemented TKA gold standard

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Conditions

Total Knee Arthroplasty

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Hospital Galdakao-Usansolo

Galdakao, Bizkaia, 48980, Spain

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Patients may be included in the study only if they meet the following criteria:

  • Patient is able to provide informed consent.
  • Patient is between 18 and 75 years of age.
  • Patients are willing and able to attend all follow-up visits and complete all study requirements. They must agree to comply with all study related procedure, including understanding and adhering to the rehabilitation protocol.
  • Patient has primary or secondary knee osteoarthritis.
  • Patient has sufficient bone quality for total knee arthroplasty.
  • Patient is in stable health.
  • Female patients are not pregnant at times of surgery and do not plan on becoming pregnant during the study.

Note: patient can only enter the project with one knee

Exclusion criteria

  • Neuromuscular or vascular disease in the affected leg.
  • Patients with osteoporosis based on former diagnosis or preoperative DEXA-scan.
  • Fracture sequelae or previous HTO or previous extensive knee surgery.
  • Patients with need of a stem-elongation.
  • Patients who cannot refrain from taking NSAID post-operatively.
  • Patients with metabolic bone disease.
  • Patients with renal disease.
  • Patients with rheumatoid arthritis.
  • Postmenopausal women in estrogenic hormone substitution
  • Patients with a continuous need of systemic cortisone treatment.
  • Non-Spanish citizenship.
  • Patients who do not comprehend the Spanish language (read and speak).
  • Senile dementia.
  • Alcohol abuse - defined as men drinking more than 21 units a week and women drinking more than 14 units a week.
  • Drug abuse.
  • Major psychiatric disease.
  • Metastatic cancer disease and treatment with radiation therapy or chemotherapy

Treatment and study plan

Total knee arthroplasty

Procedure

Use of an uncemented femoral component or a cemented femoral component randomly assigned.

NEXGEN LPS total knee arthroplasty

Device

Hybrid (non cemented femoral component, cemented tibial component) NEXGEN LPS total knee arthroplasty versus Cemented NEXGEN LPS total knee arthroplasty (both components are cemented).

Primary outcomes

  1. Postoperative functional outcome as measured by the Knee and Osteoarthritis Outcome Score (KOOS) and compare if hybrid NexGen LPS TKA leads to equally successful results as the cemented NexGen LPS TKA.

    Time frame: 1 year

    The current study will be designed as equivalence trial. The amount of allowable difference is the margin that defines the "zone of indifference" within which the interventions are considered equivalent.

    The KOOS has a Minimally Clinically Important Difference (MCID) of 8 - 10 points, and the standard deviation in a cohort of TKA patients is ca. 15 points.

    The null hypothesis (of non-equivalence) of the study is that functional outcome at 10 years of follow-up in the hybrid group is not equal to the functional outcome at 10 years of follow-up in the cemented group, or:

    H: ϑ ≤ ϑ0 - δ1 or ϑ ≥ ϑ0 + δ1, versus the equivalence assumption that functional outcome at 10 years of follow-up in the hybrid group is equivalent to the functional outcome at 10 years of follow-up in the cemented group: K: ϑ0 - δ1 < ϑ < ϑ0 + δ1.

Secondary outcomes

  1. Incidence and extend of radiolucent lines (RLL) as measured by standard radiography.

    Time frame: Up to 10 years.

    Radiography: x-rays will be taken during visit 4 and visits 7-10. Conventional anteroposterior and lateral radiographs will be taken at designated time-points. In order to obtain "true orthogonal" radiographs and to reduce the probability of false-negative findings, the lateral image will be obtained under fluoroscopic control. Postoperative radiographs will assess component position and alignment, the incidence and location of radiolucent lines using the Knee Society TKA radiographic evaluation system.

  2. Postoperative functional outcome as measured by Knee Society Score.

    Time frame: up until 10 years of follow up

    The KSS is a questionnaire validate in Spanish.The study regimen for each patient will consist of a screening / baseline phase (Visit 1), follow-up visits (Visits 3 - 9) and a conclusion visit (Visit 10). All procedures specified in this protocol must be documented in the patient's record and on the corresponding Case Report Form (CRF).

Sponsors and collaborators

Lead sponsor

Jesus Moreta Suarez

Other Gov

Registry information

Official study title

Comparing Hybrid and Cemented TKA Using the NexGen LPS Prosthesis

Important dates

Study start
2015
Primary completion
2018
Study completion
2026
First posted
Jun 14, 2016
Registry last updated
Aug 2, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.