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Evaluation of Triathlon - a New Total Knee Prosthesis System - Triathlon vs. Duracon

NCT00436982 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2024-02-22

Study results available
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Summary

The objective is to investigate the Clinical, Radiographic, Roentgen Stereophotogrammetric behaviour and patient outcome when using the Triathlon total knee prosthesis in a prospective randomized clinical trial.

Conditions

  • Arthroplasty, Replacement, Knee

Interventions

DEVICE

Cemented Triathlon total knee system

Orthopaedic implant

DEVICE

Duracon total knee system

Orthopaedic implant

Sponsors & Collaborators

  • Stryker Orthopaedics

    lead INDUSTRY

Principal Investigators

  • Sören Toksvig-Larsen, ass. prof · Department of ortopaedics, Hässleholm Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-02-28
Primary Completion
2008-11-30
Completion
2017-01-04

Countries

  • Sweden

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 NCT00436982 on ClinicalTrials.gov