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Primary Ceramic-on-Ceramic Total Hip Replacement Versus Metal-on-Metal Hip Resurfacing in Young Active Patients

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ClinicalTrials.gov Identifier: NCT00285129
Recruitment Status : Completed
First Posted : February 1, 2006
Last Update Posted : December 28, 2007
Sponsor:
Information provided by:
University Hospital, Ghent

Study Description
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Brief Summary:
Comparison of the functional result and speed of rehabilitation between two types of hip prostheses: primary ceramic-on-ceramic total hip replacement versus metal-on-metal hip resurfacing.

Condition or disease Intervention/treatment Phase
Indications for a Total Hip Prosthesis Device: ceramic-on-ceramic total hip replacement versus metal-on-metal hip resurfacing Not Applicable

Study Design
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Study Type : Interventional  (Clinical Trial)
Enrollment : 400 participants
Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Primary Ceramic-on-Ceramic Total Hip Replacement Versus Metal-on-Metal Hip Resurfacing in Young Active Patients
Study Start Date : January 2004
Actual Study Completion Date : December 2004

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Hip Replacement

Arms and Interventions
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Outcome Measures
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Primary Outcome Measures :
  1. Functional result
  2. Speed of rehabilitation

Eligibility Criteria
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Information from the National Library of Medicine

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

Inclusion Criteria:

  • Total hip replacement

Exclusion Criteria:

-

Contacts and Locations
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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): NCT00285129


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

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ClinicalTrials.gov Identifier: NCT00285129    
Other Study ID Numbers: 2004/338
First Posted: February 1, 2006    Key Record Dates
Last Update Posted: December 28, 2007
Last Verified: December 2007