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OpenTrials
Completed

NCT Number: NCT02362867

Balanced Knee System Clinical Protocol for IRB Approval

The protocol will define the clinical study for Ortho Development's Balanced Knee® System (BKS) for subsequent review and approval by an Institutional Review Board (IRB).This clinical study will compare the clinical outcomes of BKS to currently marketed devices.

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Key information

About this study

The rationale is based on the potential effectiveness of the BKS to:

  • Return patient to normal activities or increase mobility by restoring knee function.
  • Provide stability to enhance rehabilitation without external support.
  • Eliminate or reduce knee pain.
  • Assess the clinical efficacy after total knee replacement.
  • Determine implant survivorship and viability.
  • Evaluate patient function and satisfaction.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Loss of joint configuration and joint function.
  • Osteoarthritis of the knee joint.
  • Rheumatoid arthritis of the knee joint.
  • Post-traumatic arthritis of the knee joint.
  • Moderate valgus, varus, or flexion deformities.

Exclusion criteria

  • Any patient not experiencing a compromised quality of life by loss of joint function and/or joint configuration, or pain from arthritis disease.
  • Any patient whose knee cannot be returned to normal function and normal stability through reconstructive procedures, including ligamentous balancing.
  • Active infection in or near the knee joint, fever and/or local inflammation signs, and elevation of sedimentation rate unexplained by other diseases should not be treated unless preoperative infection is ruled out.
  • Distant foci of infection, such as genitourinary, pulmonary, skin (chronic lesions or ulcerations), and other sites, which may result in hematogenous spread to the implant site.
  • Rapid joint destruction or bone absorption apparent on roentgenograms.
  • Neuromuscular disorders in which the potentially adverse effects on prosthesis function are not outweighed by the benefits gained by the patient from usage of the prosthesis.
  • Mental disorders which would compromise essential patient post-operative care.
  • A painless, stable arthrodesis in a functional position.
  • Allergic reactions to implant materials, and/or tissue reactions to the products of corrosion or wear.
  • Skeletal immaturity.
  • Any patient who is unwilling or unable to comply with post-operative instructions or clinical study requirements.

Treatment and study plan

Balanced Knee System

Device

A multi-compartmental total knee replacement providing a system of components for primary posterior cruciate ligament substituting procedures. The system consists of femoral, tibial, and patellar components that allow the surgeon to select the most appropriate component combination to meet specific patient needs.

Other names: BKS

Primary outcomes

  1. Evaluate effectiveness of the BKS by assessing complications during surgery and the post-operative follow-up period

    Time frame: 1-10 years

Secondary outcomes

  1. Assess the effectiveness of the BKS by analyzing radiographic evidence and clinical data.

    Time frame: 1-10 years

  2. Identify any surveillance issues regarding the device design and surgical approach used refinement of the surgical technique

    Time frame: 1-10 years

  3. Evaluate device performance through the use of the Knee Society Score, Short Form-36 Health Survey, and radiographic evaluation.

    Time frame: 1-10 years

Sponsors and collaborators

Lead sponsor

Ortho Development Corporation

Industry

Collaborators

  • Salt Lake Orthopaedic Clinic
  • St. Mark's Hospital

Registry information

Important dates

Study start
2003
Primary completion
2019
Study completion
2019
First posted
Feb 13, 2015
Registry last updated
Sep 24, 2021

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.

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