Femoral Remodeling Following Total Hip Arthroplasty With OMNI Apex Modular™ and OMNI Apex ARC™ Stem Compared to Competitive Designs

NCT01359540 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 73

Last updated 2019-04-26

No results posted yet for this study

Summary

This study compares the change in bone density which occurs after hip replacement with different femoral stem devices.

Conditions

  • Osteoarthritis, Hip

Interventions

DEVICE

OMNI Apex Modular™ Hip Device

DEVICE

OMNI Apex ARC™ Hip Device

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
2009-11-30
Primary Completion
2018-04-30
Completion
2018-04-30

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 NCT01359540 on ClinicalTrials.gov