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Primary Birmingham Hip Resurfacing Arthroplasty Using a Metal-on-Metal Couple in the Young Active Patient

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00285948
First Posted: February 2, 2006
Last Update Posted: February 18, 2009
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
University Hospital, Ghent
  Purpose
To prospectively obtain data about the clinical and radiological results of the resurfacing technique as primary hip prosthesis in young active patients

Condition Intervention
Indications for a Total Hip Prosthesis Device: Primary Birmingham hip resurfacing arthroplasty using a metal-on-metal couple

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Primary Birmingham Hip Resurfacing Arthroplasty Using a Metal-on-Metal Couple in the Young Active Patient

Further study details as provided by University Hospital, Ghent:

Primary Outcome Measures:
  • Clinical and radiological results

Estimated Enrollment: 250
Study Start Date: November 1998
Study Completion Date: January 2009
Primary Completion Date: January 2009 (Final data collection date for primary outcome measure)
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 65 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Total hip prosthesis

Exclusion Criteria:

  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00285948


Locations
Belgium
University Hospital Ghent
Ghent, Belgium, 9000
Sponsors and Collaborators
University Hospital, Ghent
Investigators
Principal Investigator: Rene Verdonk, MD, PhD University Hospital, Ghent
  More Information

Additional Information:
Responsible Party: René Verdonk, University Hospital Ghent
ClinicalTrials.gov Identifier: NCT00285948     History of Changes
Other Study ID Numbers: 2004/339
First Submitted: February 1, 2006
First Posted: February 2, 2006
Last Update Posted: February 18, 2009
Last Verified: February 2009