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Observational Study Evaluating Outcomes of Hip Arthroplasty Using Tornier Dual Mobility Acetabular Cup

NCT02062450 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 379

Last updated 2017-05-04

Study results available
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Summary

The purpose of this study is to demonstrate the performance and reliability of Tornier "Dual Mobility Cup" used during primary total hip replacement or hip replacement revision surgery at least 24 months post-insertion.

Conditions

  • Primary Osteoarthritis
  • Post-traumatic Osteoarthritis of Hip Nos
  • Femur Head Necrosis
  • Femur Neck Fracture
  • Congenital Dislocations

Interventions

DEVICE

Primary surgery with Dual Mobility Cup

Hip joint replacement with a hip prosthesis including a Dual Mobility cup to replace the acetabular component.

DEVICE

Revision surgery with Dual Mobility Cup

Hip joint replacement with a hip prosthesis including a Dual Mobility cup to replace the acetabular component.

Sponsors & Collaborators

  • Stryker Trauma and Extremities

    lead INDUSTRY

Principal Investigators

  • Christophe Hulet, MD, PR · Caen University Hospital, FR

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-05-31
Primary Completion
2013-11-30
Completion
2013-12-31

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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 NCT02062450 on ClinicalTrials.gov