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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00285948
Other study ID # 2004/339
Secondary ID
Status Completed
Phase N/A
First received February 1, 2006
Last updated February 17, 2009
Start date November 1998
Est. completion date January 2009

Study information

Verified date February 2009
Source University Hospital, Ghent
Contact n/a
Is FDA regulated No
Health authority Belgium: Institutional Review Board
Study type Interventional

Clinical Trial Summary

To prospectively obtain data about the clinical and radiological results of the resurfacing technique as primary hip prosthesis in young active patients


Recruitment information / eligibility

Status Completed
Enrollment 250
Est. completion date January 2009
Est. primary completion date January 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Total hip prosthesis

Exclusion Criteria:

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms

  • Indications for a Total Hip Prosthesis

Intervention

Device:
Primary Birmingham hip resurfacing arthroplasty using a metal-on-metal couple


Locations

Country Name City State
Belgium University Hospital Ghent Ghent

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Ghent

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Clinical and radiological results
See also
  Status Clinical Trial Phase
Completed NCT00285129 - Primary Ceramic-on-Ceramic Total Hip Replacement Versus Metal-on-Metal Hip Resurfacing in Young Active Patients N/A