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Completed Not applicable Interventional Results available

Triathlon® Cruciate Retaining (CR) Total Knee System Outcomes Study

ClinicalTrials.gov ID: NCT00957723

Public ClinicalTrials.gov record NCT00957723. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 1:28 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Post-market, Non-randomized, Historical Controlled, Multi-center Study of the Outcomes of the Triathlon® Cruciate Retaining (CR) Total Knee System

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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® Cruciate Retaining (CR) Total Knee System. These outcomes will be evaluated by comparing pre-operative to post-operative scores, as well as to a control group. The control group is the Scorpio® CR Total Knee System.

Study identification

NCT ID
NCT00957723
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Stryker Orthopaedics
Industry
Enrollment
419 participants

Conditions and interventions

Eligibility (public fields only)

Age range
21 Years to 80 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 31, 2005
Primary completion
Mar 31, 2010
Completion
Sep 25, 2017
Last update posted
Oct 11, 2018

2005 – 2017

United States locations

U.S. sites
11
U.S. states
11
U.S. cities
11
Facility City State ZIP Site status
Arizona Institute for Bone and Joint Disorders Phoenix Arizona 85016
Cedars Medical Center University of Miami Miami Florida 33136
Hughston Sports Medicine Center Columbus Georgia 31908
Physician's Clinic of Iowa, Mercy Medical Center Cedar Rapids Iowa 52401
Newton Wellesley Hospital Newton Massachusetts 02462
Buffalo General Hospital, Department of Orthopaedics Kaleida Health Buffalo New York 14203
Crystal Clinic Akron Ohio 44330
The Center: Orthopaedic & Neurosurgical Care & Research Bend Oregon 97701
Knoxville Orthopaedic Clinic Knoxville Tennessee 37909
Scott & White Memorial Hospital Temple Texas 76508
Aurora Advanced Healthcare Milwaukee Wisconsin 53233

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00957723, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 11, 2018 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00957723 live on ClinicalTrials.gov.

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