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COMPLETED NA

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

NCT00957723 · View on ClinicalTrials.gov ↗

Study 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® 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.

Interventions

  • DEVICE Triathlon® CR Total Knee System

Study Locations (11)

Arizona

  • Arizona Institute for Bone and Joint Disorders — Phoenix

Florida

  • Cedars Medical Center University of Miami — Miami

Georgia

  • Hughston Sports Medicine Center — Columbus

Iowa

  • Physician's Clinic of Iowa, Mercy Medical Center — Cedar Rapids

Massachusetts

  • Newton Wellesley Hospital — Newton

New York

  • Buffalo General Hospital, Department of Orthopaedics Kaleida Health — Buffalo

Ohio

  • Crystal Clinic — Akron

Oregon

  • The Center: Orthopaedic & Neurosurgical Care & Research — Bend

Trial Details

FieldValue
Enrollment Target 419 participants
Start Date 2005-02
Est. Completion 2017-09-26
Phase NA

Sponsor

Stryker Orthopaedics

6 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00957723

The ClinicalTrials.gov registry entry for NCT00957723 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 419 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Stryker Orthopaedics, which has 6 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Arthroplasty, Replacement, Knee appearing as the primary indexed condition, and to 1 intervention — of which Triathlon® CR Total Knee System is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00957723 reports 11 study locations spanning 11 distinct geographic areas — top geographies include Arizona, Florida, Georgia. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00957723 about?

NCT00957723 is a clinical study titled "Triathlon® Cruciate Retaining (CR) Total Knee System Outcomes Study". 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 ...

What is the current status of trial NCT00957723?

This trial is currently completed. It is a NA study. The enrollment target is 419 participants. The study started on 2005-02. Estimated completion is 2017-09-26.

What conditions does trial NCT00957723 study?

This clinical trial studies the following conditions: Arthroplasty, Replacement, Knee. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00957723?

The interventions under investigation include: Triathlon® CR Total Knee System (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00957723?

This trial is sponsored by Stryker Orthopaedics, which has 6 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00957723 being conducted?

This trial has 11 study locations across Arizona, Florida, Georgia, Iowa, Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial