MedTrace Logo

Stryker Triathlon® Cruciate Substituting vs. Posterior Stabilized Outcomes Study

NCT01367925 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 125

Last updated 2017-12-13

No results posted yet for this study

Summary

This study compares the clinical and radiographic outcomes obtained with the use of the Stryker Triathalon® Cruciate Substituting (CS) and Posterior Stabilized (PS) tibial inserts.

Conditions

  • Osteoarthritis, Knee

Interventions

DEVICE

Stryker Triathlon® CS Tibial Insert

DEVICE

Stryker Triathlon® PS Tibial Insert

Sponsors & Collaborators

  • Spokane Joint Replacement Center

    lead OTHER

Principal Investigators

  • David F Scott, MD · Spokane Joint Replacement Center

Eligibility

Min Age
20 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2007-12-31
Primary Completion
2016-07-31
Completion
2016-07-31

Countries

  • United States

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 NCT01367925 on ClinicalTrials.gov