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Bimetric-10: Investigation of Patients Who Have Underwent Total Hip Arthroplasty With a Cemented Bi-Metric Stem

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.
 
ClinicalTrials.gov Identifier: NCT00192699
Recruitment Status : Completed
First Posted : September 19, 2005
Last Update Posted : March 31, 2014
Sponsor:
Information provided by (Responsible Party):
Northern Orthopaedic Division, Denmark

Study Description
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Brief Summary:
This is a 10 year follow-up investigation of patients who have underwent total hip arthroplasty with a cemented Bimetric stem.

Condition or disease Intervention/treatment
Osteoarthrosis Device: Bimetric femoral stem

Study Design
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Study Type : Observational
Actual Enrollment : 80 participants
Observational Model: Cohort
Time Perspective: Retrospective
Official Title: 10 Year Follow-up Investigation of Patients Who Have Underwent Total Hip Arthroplasty With a Cemented Bi-metric Stem
Study Start Date : January 2004
Actual Primary Completion Date : April 2011
Actual Study Completion Date : April 2011

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Osteoarthritis

Groups and Cohorts
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Group/Cohort Intervention/treatment
Group 1: Cemented Bi-Metric femoral stem
Cemented Bi-Metric femoral stem
 Device: Bimetric femoral stem
Cemented Bi-Metric femoral stem
Other Name: Cemented Bi-Metric femoral stem


Outcome Measures
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Eligibility Criteria
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Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients with osteoarthrosis in hip who have underwent surgery for 10 years ago using Cemented Bi-Metric femoral stem.
Criteria

Inclusion criteria:

  • Osteoarthrosis

Exclusion criteria:

  • Malignancies
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): NCT00192699


Locations
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Denmark
Northern Orthopaedic Division, Aalborg University Hospital
Aalborg, Northern Jutland, Denmark, 9000
Sponsors and Collaborators
Northern Orthopaedic Division, Denmark
Investigators
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Principal Investigator: Mogens B Laursen, MD, PhD Northern Orthopaedic Division, Aalborg University Hospital, Denmark
More Information
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Responsible Party: Northern Orthopaedic Division, Denmark
ClinicalTrials.gov Identifier: NCT00192699    
Other Study ID Numbers: ON-04-008b-JPE
First Posted: September 19, 2005    Key Record Dates
Last Update Posted: March 31, 2014
Last Verified: March 2014
Keywords provided by Northern Orthopaedic Division, Denmark:
Osteoarthritis
Additional relevant MeSH terms:
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Osteoarthritis
Arthritis
Joint Diseases
Musculoskeletal Diseases
Rheumatic Diseases