MedTrace Logo

Clinical Outcome Study for the Triathlon Cruciate Retaining (CR) Total Knee

NCT02535741 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 168

Last updated 2024-02-22

Study results available
· View outcomes & findings →

Summary

An open label, post-market, non-randomised, historical controlled, multi-centre study of the outcomes of the Triathlon Cruciate Retaining (CR) Total Knee System.

Conditions

  • Total Knee Arthroplasty

Interventions

DEVICE

Triathlon CR Total Knee System

Primary total knee replacement

Sponsors & Collaborators

  • Stryker Orthopaedics

    lead INDUSTRY

Principal Investigators

  • Christina Stukenborg-Colsman, Prof. · Medizinische Universität Hannover

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
2006-10-31
Primary Completion
2013-05-31
Completion
2016-05-31

Countries

  • Denmark
  • Finland
  • Germany
  • Spain

Study Locations

More Related Trials

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 NCT02535741 on ClinicalTrials.gov