Triathlon® Posteriorly Stabilized (PS) Total Knee System - Outcomes Study

NCT00957021 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 409

Last updated 2017-01-25

Study results available
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Summary

The purpose of this study is to evaluate the clinical outcomes (range of motion, pain, function, radiographic stability, and health related quality of life) of patients receiving the Triathlon® Posterior Stabilized (PS) Total Knee System. These outcomes will be evaluated using pre-operative scores and comparing them to post-operative scores in addition to being compared with cases who received the Scorpio® PS implant.

Conditions

  • Arthroplasty, Replacement, Knee

Interventions

DEVICE

Triathlon® PS Total Knee System

Triathlon® PS Total Knee system

Sponsors & Collaborators

  • Stryker Orthopaedics

    lead INDUSTRY

Principal Investigators

  • Eric R Benson, MD · New Hampshire Orthopaedic Surgery, PA

  • Daniel Moretta, DO · Tri County Orthopedics Surgeons, Inc.

  • James Bono, MD · New England Baptist Hospital

  • David W Edelstein, MD · Kelsey-Seybold Clinic

  • Philip Ireland, MD · Ireland Hip and Knee Surgery

  • Joseph P Nessler, MD · St. Cloud Orthopaedic Associates

  • Quanjun Cui, MD · University of Virginia

  • Arnold Scheller, MD · Pro-Sports Orthopaedics, Inc./ New England Baptist Hospital

  • Joel Sorger, MD · Wellington Orthopaedics and Sports Medicine

  • Suresh Nayak, MD · Wellington Orthopaedics and Sports Medicine

  • John I Waldrop, MD · Hughston Clinic, PA

  • James McGrory, MD · Hughston Clinic, PA

  • Steven B Zelicof, MD, PhD · Specialty Orthopaedics

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
21 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-12-31
Primary Completion
2011-03-31
Completion
2014-01-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00957021 on ClinicalTrials.gov