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Optetrak Posterior Stabilized Versus Optetrak Hi-Flex

NCT00808613 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2022-09-01

No results posted yet for this study

Summary

The purpose of this study is to evaluate the differences in clinical outcomes between the Optetrak® Posterior Stabilized ("Optetrak® PS", Exactech, Gainesville, FL) and the Optetrak® Hi-Flex™ ("Optetrak® HF", Exactech, Gainesville, FL) knee designs.

Conditions

  • Arthropathy of Knee
  • Arthritis and/or Post-traumatic Degenerative Problems

Interventions

DEVICE

Optetrak PS

Optetrak Posterior Stabilized total knee replacement

DEVICE

Optetrak Hi-Flex

Optetrak Hi-Flex total knee replacement

Sponsors & Collaborators

  • Exactech

    lead INDUSTRY

Principal Investigators

  • Jason Drenning, Ph.D. · Exactech

  • John W. Aldridge, MD · Hampton Roads Orthopedics

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
50 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-12-31
Primary Completion
2012-01-31
Completion
2012-01-31

Countries

  • United States

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 NCT00808613 on ClinicalTrials.gov