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Post-Market Study of the Modular Revision Hip System

NCT01464645 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 16

Last updated 2018-10-10

No results posted yet for this study

Summary

The purpose of this study is to examine the short term efficacy of the MRH system as well as determine if operating room time is decreased using this simple, two-tray system.

Conditions

  • Aseptic Loosening
  • Osteolysis
  • Traumatic Fracture
  • Failed Total Hip Implant

Interventions

DEVICE

Modular Revision Hip System

Hip System that is indicated for patients whose bone stock is of poor quality or inadequate for other reconstruction techniques as indicated by deficiencies of the femoral head, neck or portions of the proximal femur.

Sponsors & Collaborators

  • DJO Incorporated

    collaborator INDUSTRY

  • Encore Medical, L.P.

    lead INDUSTRY

Principal Investigators

  • Michael Levine, M.D. · Orthopedic Associates of Pittsburgh, Inc.

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-01-31
Primary Completion
2017-12-31
Completion
2017-12-31

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 NCT01464645 on ClinicalTrials.gov