Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

COMPLETED NA

Clinical Investigation of the LCS® Complete Posterior Stabilized Mobile-bearing Total Knee System

NCT00487565 · View on ClinicalTrials.gov ↗

Study Summary

Prospective, multi-center clinical study to evaluate the clinical outcomes of the posterior stabilized design of the LCS® Complete Mobile-bearing Total Knee System

Interventions

  • DEVICE Total knee arthroplasty

Study Locations (3)

Colorado

  • Colorado Joint Replacement — Denver

Pennsylvania

  • Joint Reconstruction Center — Pittsburgh

Virginia

  • Jordan-Young Institute — Virginia Beach

Trial Details

FieldValue
Enrollment Target 210 participants
Start Date 2006-09
Est. Completion 2011-02
Phase NA

Sponsor

DePuy Orthopaedics

43 total trials

Interested in This Trial?

Always speak with your doctor before enrolling in a clinical trial.

Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00487565

The ClinicalTrials.gov registry entry for NCT00487565 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 210 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is DePuy Orthopaedics, which has 43 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 4 conditions, with Rheumatoid Arthritis appearing as the primary indexed condition, and to 1 intervention — of which Total knee arthroplasty 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: NCT00487565 reports 3 study locations spanning 3 distinct geographic areas — top geographies include Colorado, Pennsylvania, Virginia. 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 NCT00487565 about?

NCT00487565 is a clinical study titled "Clinical Investigation of the LCS® Complete Posterior Stabilized Mobile-bearing Total Knee System". Prospective, multi-center clinical study to evaluate the clinical outcomes of the posterior stabilized design of the LCS® Complete Mobile-bearing Total Knee System

What is the current status of trial NCT00487565?

This trial is currently completed. It is a NA study. The enrollment target is 210 participants. The study started on 2006-09. Estimated completion is 2011-02.

What conditions does trial NCT00487565 study?

This clinical trial studies the following conditions: Rheumatoid Arthritis, Osteoarthritis, Post-traumatic Arthritis, Juvenile Arthritis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00487565?

The interventions under investigation include: Total knee arthroplasty (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00487565?

This trial is sponsored by DePuy Orthopaedics, which has 43 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00487565 being conducted?

This trial has 3 study locations across Colorado, Pennsylvania, Virginia. 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