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Clinical Trials/NCT00958789
NCT00958789CompletedNot Applicable

A Prospective, Post-market, Multi-center Study of the Outcomes of the Triathlon® Total Stabilizer (TS) Total Knee System

Stryker Orthopaedics24 sites in 1 country180 target enrollmentStarted: July 2009Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
180
Locations
24
Primary Endpoint
Knee Society Score (KSS) Change From Preoperative Time Point to 2 Years

Study Overview

Brief Summary

This study will be a prospective, non-randomized evaluation of the change between preoperative and postoperative outcomes for those receiving the Triathlon® TS Total Knee System for a revision knee operation. The mean total Knee Society Score (for pain, motion and function) change is not 10% worse than, or is superior to, the expected change according to published revision total knee replacement data, for cases implanted with the Triathlon® TS Total Knee System as compared from preoperative to 2 years postoperative.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

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

Inclusion Criteria

  • Patient has signed an Institutional Review Board (IRB) approved, study specific Informed Patient Consent Form.
  • Patient is a male or non-pregnant female age 18 years or older at time of study device implantation.
  • Patient is a candidate for revision of all femoral and tibial components of a total knee replacement.
  • Patient is willing and able to comply with postoperative scheduled clinical and radiographic evaluations and rehabilitation.

Exclusion Criteria

  • Patient has a Body Mass Index (BMI) >
  • Patient has an active or suspected latent infection in or about the affected knee joint at time of study device implantation.
  • Patient has a neuromuscular or neurosensory deficiency, which limits the ability to evaluate the safety and efficacy of the device.
  • Patient is diagnosed with a systemic disease (e.g. Lupus Erythematosus) or a metabolic disorder (e.g. Paget's Disease) leading to progressive bone deterioration.
  • Patient is immunologically suppressed or receiving steroids in excess of normal physiological requirements (e.g. > 30 days).
  • Patient has a failed unicondylar knee prosthesis.
  • Patient has a known sensitivity to device materials.
  • Patient is a prisoner.

Outcomes

Primary Outcomes

Knee Society Score (KSS) Change From Preoperative Time Point to 2 Years

Time Frame: pre-op, 2 years

KSS Pain score, KSS Function score, Total Combined KSS The Knee Society Clinical Rating System is comprised of two distinct sub-scores: one for pain, range of motion (ROM) and joint stability, and one for functional parameters. Sub-scores range from a potential minimum score of 0 to a maximum score of 100 points. Although the specific scores are not distinguished as "excellent," "good," "fair," or "poor," a higher value represents a better outcome. Additionally, the KSS Pain subscore and KSS Function subscore are added together to obtain a total combined score (minimum score 0, maximum score 200).

Secondary Outcomes

  • Short Form Health Survey (SF-36) Health Survey Change From Pre-op to Post-op Visits(pre-op, 1, 2, 5 years)
  • Knee Stability Results Stratified by Joint Line Restoration Groups at 2 and 5 Year Postoperative(2 year and 5 year postoperative)
  • Hospital Special Surgery (HSS) Patella Score Change From Pre-op to Post-op Visits(pre-op, 1, 2, 5 years)
  • Lower Extremity Activity Scale (LEAS) Score Change From Pre-op to Post-op Visits(pre-op, 1, 2, 5 years)
  • Number of Knees With a Revision of Femoral and/or Tibial Baseplate Component(5 years)
  • Knee Society Score (KSS) Functional Results Stratified by Joint Line Restoration Groups at 2 and 5 Years Postoperative(2 years, 5 years)
  • Anterior Knee Pain Results Stratified by Joint Line Restoration Groups at 2 and 5 Years Postoperative(2 year and 5 year postoperative)
  • Knee Injury and Osteoarthritis Outcome Score (KOOS) Change From Pre-op to Post-op Visits(pre-op, 1, 2, 5 years)
  • Knee Society Score (KSS) Change From Pre-op to Post-op Visits(pre-op, 1,2, 5 year)
  • Number of Knees With Radiographic Stability at 1, 2 and 5 Years Postoperative(1, 2, 5 years)

Investigators

Sponsor Class
Industry
Responsible Party
Sponsor

Study Sites (24)

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